Import Procedure for Oral Beauty Products

ORAL BEAUTY PRODUCT | FOOD / HEALTH SUPPLEMENT

IMPORT PROCEDURE FOR ORAL BEAUTY PRODUCTS

This article applies to oral beauty products such as collagen drinks, beauty drinks, skin-support capsules, sachets, gummies or supplements claiming beauty-from-within benefits. Before ETA, importers should lock product classification, HS code, duties, C/O, product declaration, imported food safety inspection, Vietnamese supplementary labeling and claims to avoid dossier supplementation, loss of C/O preference or storage costs.

Legal note. An oral beauty product is not an external-use cosmetic. Depending on ingredients, dosage form and claims, it may be regulated as a health supplement, supplemented food, non-alcoholic beverage, or may trigger drug-boundary review if it claims to treat acne, melasma or disease. Review catalogue, formula, label, COA, CFS/GMP and actual import purpose.

QUICK FACT TABLE

ITEM REVIEW POINTS
Product Oral beauty product – beauty drink, collagen drink, oral skin-support supplement, collagen/vitamin/mineral/probiotic product or bioactive supplement for oral use.
Key legal classification Usually reviewed as health supplement / functional food / supplemented food. If circulated as a common beverage, a different procedure may apply; therapeutic claims may require reclassification.
Reference HS codes 2106.90.70 – food supplements; 2202.90.50 – other non-aerated beverages ready for immediate consumption without dilution; 2202.90.90 – other non-alcoholic beverages.
Reference taxes 2106.90.70: MFN 15%, VAT 10%; 2202.90.50: MFN 30%, ordinary duty 45%, VAT 10%; 2202.90.90: MFN 20%, ordinary duty 30%, VAT 10%. Verify at declaration date.
Specialized dossier Product declaration registration or self-declaration depending on classification; imported food safety inspection; CFS/Health Certificate/GMP if health supplement; COA/testing result; Vietnamese supplementary label.
Typical hold points Therapeutic claims, missing product declaration receipt, missing CFS/GMP, labels without the “not a medicine” disclaimer, and C/O with wrong HS or description.

SCOPE OF APPLICATION

This article applies only to oral beauty products within a sensitive regulatory boundary between cosmetics, health supplements and products with therapeutic claims. It does not apply automatically to acne drugs, disinfectants, beauty devices or external-use cosmetics.

  • Applies to bottled collagen drinks, cans, stick packs, sachets, oral ampoules, capsules, tablets or gummies.
  • Applies to commercial imports, testing samples, R&D samples, imports for EPE/FDI/factories, and promotional products placed on the market.
  • Does not automatically apply to alcoholic beverages, drugs, external-use cosmetics, medical foods, infant products or products with specially controlled substances.
  • If claims include “treat acne”, “cure melasma”, “anti-inflammatory” or “antibacterial from within”, classification must be reviewed before import.

Review is required based on catalogue, formula, nutrition facts, label, COA, CFS/GMP, packaging form and actual import purpose.

CLASSIFICATION & TECHNICAL IDENTIFICATION

Technical identification

  • Product form: collagen drink, powder for drink, capsule, tablet, gummy, oral ampoule.
  • Main ingredients: collagen peptide, vitamin C, biotin, zinc, hyaluronic acid, probiotics, botanical extracts, sweeteners, flavours.
  • Claims: supports skin beauty, antioxidant support, collagen supplementation, skin health support; therapeutic claims must be removed or reclassified.
  • Usage: oral use, dosage, target users, warnings and contraindications if any.
  • Market form: bulk, retail, sample, combo, promotion or testing product.

Do not describe it as cosmetics

Oral-use products should not be declared under Chapter 33 merely because they relate to beauty. A vague description such as “cosmetic drink” may cause wrong HS classification, wrong declaration route and food safety inspection issues.

Criterion Documents to verify Risk if misdescribed Suggested customs/commercial description
Product form Catalogue, label, packing photo Confusion between common beverage and health supplement Beauty supplement drink / collagen drink, ready-to-drink, bottle … ml
Active ingredients Formula, COA, nutrition facts Wrong HS or missing food safety dossier Food supplement containing collagen peptide, vitamin C …
Claims Label, leaflet, web claims Drug-boundary review Use support claims only; avoid treatment wording
Declaration classification Product declaration, CFS, GMP, test report Wrong authority or incomplete dossier Imported health supplement under registered declaration

HS CODE – DUTIES – C/O

HS classification depends on product form, ingredients, use and claims. Do not lock an HS code solely from the trade name “beauty drink”.

Reference HS Applicable case Risk if wrong Documents to verify
2106.90.70 Food supplements: capsules, sachets, collagen supplements, bioactive oral beauty supplements. Wrong if circulated primarily as a beverage or as a drug. Formula, COA, label, product declaration, CFS/GMP.
2202.90.50 Non-aerated ready-to-drink beverage for immediate consumption without dilution. Higher MFN duty and possible mismatch with supplement declaration. Label, usage, nutrition facts, declaration dossier.
2202.90.90 Other non-alcoholic beverages not fitting a more specific subheading. Insufficient basis if the product is clearly a food supplement. Catalogue, label, ingredients, declaration dossier.
3004 / pharmaceutical headings Only if active ingredients and therapeutic presentation indicate drug treatment. Food procedure may be invalid. Claims, actives, clinical documents, label and drug permit if applicable.
HS scenario Reference MFN Reference ordinary duty VAT Conditions
2106.90.70 – Food supplements 15% 22.5% if no separate ordinary rate is available 10% For oral supplements/health supplements after checking formula and declaration dossier.
2202.90.50 – Non-aerated ready-to-drink beverage 30% 45% 10% For ready-to-drink non-alcoholic beverages not falling under fruit juice heading 20.09.
2202.90.90 – Other non-alcoholic beverage 20% 30% 10% For other non-alcoholic beverages depending on formula and description.
Valid C/O Special preferential duty may apply if the C/O/origin document, HS code, description, origin criterion and direct transport conditions are valid.

C/O / FTA preferential duty review

Origin route Form / origin document Preferential duty to verify Conditions Risk
ASEAN Form D or ATIGA origin document 2106.90.70 often has an ATIGA 0% line if origin rules are met; 2202.90.xx must be checked by exact 8-digit HS. Correct form, HS, goods description, origin criterion and direct transport. Preference may be rejected if the C/O describes the goods too generally or shows mismatched HS/quantity.
China Form E under ACFTA or RCEP origin document Compare ACFTA and RCEP by exact HS; do not apply one rate to all 2106 and 2202 products. Review CTH/RVC, third-party invoice, transit and ingredient description. Wrong form or origin criterion may result in MFN/ordinary duty and tax adjustment.
Korea Form AK, Form VK or RCEP Deep preference may apply; select the lowest valid agreement at declaration date. Check producer, origin criterion, third-party invoice and C/O issuance date. Wrong form or expired C/O may shift the shipment back to MFN.
Japan Form AJ, Form VJ, CPTPP or RCEP Under CPTPP, Viet Nam’s schedule shows 2106.90.70 under B5 staging and reaching 0% after staging; verify the currently effective schedule. Review self-certification, origin criterion and direct transport. Preference is not available if the goods do not meet the origin rule.
EU EUR.1 or EVFTA origin statement Check EVFTA rate by exact 8-digit HS; do not generalize across all beauty drinks or supplements. Check exporter statement, REX where applicable, goods description and origin country. Wrong origin wording, HS or transport evidence may reject preference.
UK UKVFTA origin declaration Check by 8-digit HS at declaration date; preference depends on valid origin declaration. Review invoice origin statement, description, origin criterion and transport route. A commercial invoice without valid origin wording is insufficient.
Australia/New Zealand AANZFTA, CPTPP or RCEP AANZFTA provides deep preference for 2106.90.70; compare against CPTPP/RCEP for the actual shipment. Select the best agreement only if the respective origin rule is met. Wrong agreement selection or missing direct-transport proof may reject preference.
India Form AI Check by exact HS; do not assume 0% for all food supplements. Review RVC/CTH, ingredients and production process. Wrong origin criterion may invalidate AIFTA preference.
No C/O Not applicable MFN may apply if conditions are met; otherwise ordinary duty may apply, e.g. 22.5% for MFN 15%, 45% for MFN 30%. Review origin, purchase terms and landed cost before ordering. Higher landed cost, especially under 2202.90.50.

Pre-ETA C/O checklist

Checkpoint What to verify Risk if missed
Form / origin document Correct agreement: Form D, E, AK, VK, AJ, VJ, AI, EUR.1, CPTPP/RCEP/UKVFTA declaration… Wrong form may lose preferential duty.
Origin criterion WO, RVC, CTH/CTSH under the relevant agreement. A correct form with wrong criterion can still be rejected.
HS and description HS and goods description must match invoice, packing list, label and customs declaration. Mismatch may trigger consultation or duty adjustment.
Third-party invoice If used, the C/O must show the required indication/box for the relevant agreement. The C/O may be challenged or rejected.
Direct transport Review B/L/AWB, transit route and non-manipulation evidence if transshipment occurs. Failure to prove direct transport may lose preference.
Quantity, weight, issue date Must match the commercial documents and remain valid. Customs may request correction before clearance.

APPLICABLE SPECIALIZED POLICIES

Goods scenario Potential policy Documents Authority/portal Timing Risk note
Imported health supplement Registered product declaration before circulation/import for commercial sale CFS/Health Certificate, GMP, test report, label, formula Ministry of Health / Vietnam Food Administration online public service Before commercial shipment Missing receipt may block clearance or circulation.
Common supplemented beverage Self-declaration or registration depending on product nature Test result, declaration, label Local food safety authority or MOH Before market placement Wrong filing authority delays the dossier.
Therapeutic claims Drug-boundary review Claim matrix, active ingredients, label, leaflet MOH and competent departments Before contract and label printing Functional foods must not claim to cure disease.
Testing/R&D samples Proper HS, value and purpose declaration; possible specialized review Sample invoice, PO, technical documents Customs / food safety authority if requested Before ETA Do not assume automatic exemption.

LEGAL DOCUMENTS TO REVIEW

Group Document Issuer Effectiveness Role Key points Review note
Law Law on Food Safety No. 55/2010/QH12 National Assembly Check current validity Framework for food safety and labeling Food labeling and safety obligations No disease-treatment claim for foods.
Decree Decree 15/2018/ND-CP Government Currently applied; check amendments Product declaration and imported food safety inspection Articles 6, 7, 8 and annexes Health supplements are usually registered with MOH.
Circular Circular 43/2014/TT-BYT Ministry of Health Effective from 15 Jan 2015 Management of functional foods Scope, definitions, labeling and usage instructions Check “not a medicine” disclaimer.
Labeling Decree 43/2017/ND-CP and Decree 111/2021/ND-CP Government Decree 111 effective from 15 Feb 2022 Goods labeling and Vietnamese supplementary labels Mandatory label contents Supplementary label must match declaration dossier.
Tariff/VAT Decree 108/2025/ND-CP and Decree 174/2025/ND-CP Government 108 effective 19 May 2025; 174 effective 01 Jul 2025 Import tariff and VAT reduction review Chapters 21, 22 and VAT exclusion annexes Do not finalize tax without confirming 8-digit HS.

VIEW / DOWNLOAD SOURCE DOCUMENTS

Enterprises should cross-check source documents on official legal databases or issuing authority websites before applying them.

CUSTOMS CLEARANCE DOSSIER

Commercial documents

  • Commercial Invoice and Packing List.
  • Bill of Lading / Air Waybill.
  • Sales Contract / Purchase Order.
  • C/O if preferential duty is claimed.
  • Catalogue, original label, product photos and SKU list.

Specialized documents

  • Registered product declaration receipt or self-declaration if applicable.
  • COA/testing report for food safety indicators.
  • CFS/Health Certificate/GMP for imported health supplements if applicable.
  • Vietnamese supplementary label and claim documents.
  • Imported food safety inspection dossier.
Dossier group Required documents Used for Prepared by Common errors Pre-ETA check
Commercial Invoice, PL, B/L/AWB, contract Customs value and transport Supplier, importer, forwarder Product name differs from declaration Match product name, SKU and quantity.
Declaration Product declaration/self-declaration Proof of eligibility for import/circulation Importer, regulatory team Dossier unfinished when goods arrive Complete before commercial shipment.
Testing COA, test report Declaration and food safety inspection Supplier, lab, importer Missing safety indicators Compare indicators against declaration dossier.
Labeling Original label, supplementary label, artwork Market circulation Brand owner, importer Therapeutic wording or missing disclaimer Review artwork before import.

DECISION POINTS THAT MAY HOLD THE SHIPMENT

Decision point Question Evidence Consequence Recommended handling
Product classification Health supplement, supplemented food or beverage? Label, formula, declaration, claims Supplementary dossier or reclassification Lock classification before contract.
HS code 2106.90.70 or 2202.90.xx? Formula, dosage form, label Wrong duty, C/O and policy Match HS with product form and declaration.
Claims Any treatment/disease claim? Label, website, leaflet Drug-boundary review Use support claims only.
C/O Correct HS, description and form? C/O draft, invoice, B/L Loss of preferential duty Review C/O before issuance.

PRACTICAL E2E PROCESS

  1. Pre-ETA review: lock classification, HS, duties, C/O, claims, label, declaration and food safety requirements.
  2. Document lock: invoice, PL, B/L/AWB, C/O, catalogue, label, COA, CFS/GMP and product declaration.
  3. Specialized filing: complete product declaration/self-declaration and imported food safety inspection where applicable.
  4. Customs declaration: control value, HS, product description, C/O and specialized dossier; handle green/yellow/red channels.
  5. Clearance and delivery: obtain D/O, inspect goods, deliver to warehouse and apply supplementary labels before distribution.
  6. Post-clearance archive: keep declaration, tests, C/O, import dossier, label and claim documents.

PRE-ETA RISK CHECKLIST

Risk Consequence Pre-ETA control Documents
Therapeutic claim Reclassification or circulation issue Review all labels, websites and ads Label, leaflet, claim matrix
Missing declaration Clearance/circulation delay Complete before commercial shipment Declaration receipt
Wrong 2106/2202 HS Wrong duties and C/O Review formula, form and usage Formula, COA, label
C/O error No preferential duty Check draft C/O before ETA C/O, invoice, B/L
Label mismatch Relabeling or market delay Compare label with declaration Original and supplementary labels

FAQ – COMMON BUSINESS QUESTIONS

Question Short answer
Is an oral beauty product a cosmetic? Usually no. Oral products are reviewed under food/health supplement or beverage regulations depending on formula and claims.
Is a cosmetic notification required? Generally no for oral products; a food/health supplement declaration route should be reviewed.
Should HS be 2106.90.70 or 2202.90.50? It depends on whether the product is a food supplement or ready-to-drink beverage.
Can the label say “treat acne from within”? Treatment claims should be avoided for foods and must be reviewed carefully.
Can C/O reduce duty? Yes, if the origin document is valid and matches HS, description and origin rules.
Is VAT 8% or 10%? Base VAT is commonly 10%; any 8% reduction must be checked against Decree 174/2025 and exclusion annexes at declaration date.

RELATED ARTICLES

IMPLEMENTATION SOLUTION FROM TGIMEX

This article outlines HS code, duties, dossiers and specialized policies for oral beauty products. In real shipments, importers still need to review formula, label, claims, COA, CFS/GMP, documents, origin and import purpose.

Coordination capability

  • Agent network in more than 60 countries.
  • Member of WCA, WCA China Global, VLA and HNLA.
  • Sea, air, road and rail logistics.
  • Customs clearance, C/O, permits, warehousing and domestic transport.

Support scope

  • Pre-ETA review: HS, policy, C/O, duties, label, claims and food safety dossier.
  • Compliance control: invoice, PL, B/L/AWB, C/O, COA, CFS/GMP and declaration dossier.
  • Coordination with agents, carriers, ETA and pre-alert.
  • Customs declaration, green/yellow/red channel handling and post-clearance archiving.

For shipments that may involve specialized inspection, permits, C/O or labeling requirements, enterprises should not wait until cargo arrival to start dossier review. Even a minor discrepancy between invoice, packing list, catalogue, datasheet, C/O or label may trigger additional document requests, delayed clearance or unplanned storage costs.

QUICK CONSULTATION

NEED TO REVIEW IMPORT PROCEDURES OR A SHIPPING PLAN?

Send us the product name, shipping route, current dossier, or implementation request in advance so we can suggest a suitable approach that is practical, focused, and aligned with your shipment.

CALL NOW
Zalo
HOTLINE 0963 856 664 / 0982 135 393
EMAIL info@tgimex.com
SUITABLE FOR International shipping · Customs procedures · Import licenses · B2B logistics

Leave a Reply

Discover more from TGIMEX VIETNAM JSC

Subscribe now to keep reading and get access to the full archive.

Continue reading