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Colombia Cosmetic Registration

11 月 26, 2025 Registration Insights 0 views

1. Regulatory Authority & Framework

Cosmetics in Colombia are regulated by:

  • Decreto 677 de 1995
  • Decreto 219 de 2022
  • Resolución 1482 de 2021
  • Andean Community (CAN) Decisions 516 & 833
  • INVIMA – National Institute for Food and Drug Surveillance

Colombia follows the Andean Community harmonized cosmetic regulations (Bolivia, Ecuador, Peru, Colombia).

Legally, cosmetics require a Notificación Sanitaria Obligatoria (NSO) before commercialization.

2. Definition of Cosmetic (CAN Decision 516)

Product intended to contact external body parts for:

  • Cleansing
  • Perfuming
  • Modifying appearance
  • Protecting
  • Maintaining condition

If the product has therapeutic or physiological modification claims, it becomes:

  • Health Product,
  • Drug, or
  • Medical Device,
    not a cosmetic.

3. Type of Registration Required

Cosmetics → Notificación Sanitaria Obligatoria (NSO)

This is a mandatory pre-market notification, similar to Brazil Class I or EU CPNP.

Output:

  • NSO number
  • Validity: 7 years
  • Must be updated if changes occur in:
    • Formula
    • Manufacturer
    • Name/branding
    • RP/importer details

NSO is required before importation or sale.

4. Who Can Apply? – Colombian Legal Representative (RP) Required

Foreign manufacturers cannot apply directly.

An importer or distributor based in Colombia must serve as:

  • Titular (Owner) of NSO, and
  • Responsible Person under Colombian law

Responsibilities:

  • Submit NSO
  • Maintain technical documentation
  • Handle adverse event reports
  • Manage recalls and communication with INVIMA

Changing the RP requires modifying the NSO.

5. NSO Dossier Requirements

A. Administrative Requirements

  • Completed NSO form
  • Proof of payment of renewal/applicant fees
  • Power of Attorney (if RP submits on behalf of manufacturer)

B. Technical Requirements

Similar to an internal PIF under EU rules:

  1. Product description
  2. Full qualitative & quantitative formula (%)
  3. Ingredient safety data (toxicology)
  4. Manufacturing process
  5. ISO 22716 GMP certificate (mandatory for manufacturer)
  6. Stability studies
  7. Microbiological limits testing
  8. Packaging material compatibility
  9. Label artwork
    • Spanish compliance
  10. Claims substantiation

Note: Documents are submitted directly to INVIMA (not kept internally like Canada/Mexico).

6. Ingredient Restrictions (CAN Harmonized List)

Colombia follows Andean Community Ingredient Lists, harmonized with the EU:

  • Prohibited ingredients (similar to EU Annex II)
  • Restricted ingredients (Annex III-type)
  • Approved preservatives
  • Approved UV filters
  • Approved colorants

Common prohibitions:

  • Hydroquinone (cosmetic)
  • Mercury compounds
  • Corticosteroids
  • Prescription retinoids
  • Strong bleaching agents

Warnings required for:

  • Hair dyes
  • AHA
  • Salicylic acid
  • Peroxide-based products

7. Labeling Requirements (Spanish Mandatory)

Under INVIMA + CAN Resolution 833, labels must include:

  • Product name & cosmetic category
  • Function & usage instructions
  • Ingredient list (INCI)
  • Lot/batch number
  • Manufacturing & expiry date
  • Country of origin
  • Name & address of NSO Holder (RP)
  • Net content
  • Warnings (for restricted ingredients)

Spanish is mandatory on the label.
Stickers for imported products are accepted.

8. Fees & Timelines

Government Fees (approximate)

  • NSO application: ~USD 300–350
  • Modification: ~USD 100
  • Renewal (every 7 years): ~USD 250–300

Fees may vary depending on product subtype.

Timelines

  • Preparation of dossier: 1–2 weeks
  • INVIMA review: 2–6 weeks
  • Validity: 7 years

Colombia has one of the longest-validity cosmetic authorizations in LATAM.

9. Importation Requirements

Before importation, you must have:

  • Valid NSO number (mandatory)
  • Label aligned with Colombian standards
  • Import license (from importer)
  • Commercial invoice & packing list
  • Product samples (for customs inspection if requested)

INVIMA may perform:

  • Border inspections
  • Sampling for microbiology or heavy metals
  • Label compliance review

10. Post-Market Surveillance (PMS)

INVIMA enforces strict PMS:

  • Market inspections
  • Laboratory testing
  • Claims evaluation
  • Recall orders and sanctions
  • Online advertising monitoring
  • Manufacturer/importer audits

RP (Titular) must:

  • Maintain tech documentation
  • Report adverse events
  • Conduct recalls when required

11. Borderline Product Classification

Product TypeColombia ClassificationNotes
Whitening creamsCosmeticAvoid medical “melasma” claims
SunscreensCosmetic (with UV filters)Must use approved UV filters; claims substantiation required
Anti-acneDrugBPO, BP, SA high doses → Not cosmetic
Hair dyesCosmeticWarning labels needed
Anti-hair lossHealth ProductRequires Sanitary Registration
Anti-dandruffDrugKetoconazole allowed only as drug
Sheet masksCosmeticMust meet preservative rules
AHA/BHA treatmentsCosmetic or borderlineConcentration limits apply

12. Consulting Notes for Your Portfolio

ProductColombia CategoryKey Notes
Brightening/whitening serumCosmeticAvoid therapeutic claims
SunscreensCosmeticUV filter compliance required
Anti-acneDrugNot eligible for NSO
Hair growth tonicsNot cosmeticRequires medicinal registration
Sheet masksCosmeticEnsure microbiology compliance
AR/MR medical systemsDeviceNot cosmetic

13. Advantages of the Colombian Cosmetic Market

  • Harmonized with Andean Community (Peru, Ecuador, Bolivia) → easy expansion
  • Long validity (7 years)
  • Predictable INVIMA procedures
  • Strong beauty and personal-care market
  • High consumer trust for Korean/Japanese/European/Chinese skincare

Author:Grzan

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