Is HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA safe to use in EU cosmetics?

HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA appears in the EU CosIng inventory and has linked annex records. Check the annex records for applicable restrictions, concentration limits and conditions of use. Annex II means prohibited; Annex III means restricted; Annexes IV, V and VI mean permitted under specified conditions.

InventoryRef 9563513/12/2018

HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA

Q: How do I check if my formula contains HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA?

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HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA is linked to 1 EU annex record on this page. Inventory note: II/416.

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Inventory details for HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA

INCI name

HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA

Description

Human Neonatal Fibroblast/Keratinocyte Conditioned Media is the growth media removed from cultures of human neonatal fibroblasts and human neonatal keratinocytes after several days of growth.The starting media is Minimum Essential Medium Eagle with Earle's salts without L-glutamine and phenol red, and may or may not contain fetal bovine serum.

Annex records for HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA

Annex II Restriction reference

Entry 416

Cells, tissues or products of human origin

Key data

CAS

—

Restriction

II/416

Function

SKIN CONDITIONING

How HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA appears in the CosIng inventory

The CosIng inventory lists HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA as a cosmetic ingredient and this page links it to 1 annex record. The inventory entry captures names and identifiers, while the annex record shows where the substance is prohibited, restricted or positively listed in EU cosmetics law.

HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA is also tagged with 1 cosmetic function in the official data. Function labels describe intended use, but they do not replace regulatory review of linked annex records before formulation or labelling work.

Frequently asked questions

HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA appears in the EU CosIng inventory and has linked annex records. Check the annex records above for applicable restrictions, concentration limits and conditions of use. Annex II listing means prohibited; Annex III means restricted; Annexes IV, V and VI mean permitted under specified conditions.

The restriction field for HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA reads: "II/416". This is the restriction note recorded in the CosIng inventory for this ingredient. For authoritative conditions and limits, always refer to the linked annex entries above.

According to the EU CosIng inventory, HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA carries the following function designation(s):

SKIN CONDITIONING

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Source note for HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA

This page combines the CosIng inventory entry for HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA with 1 linked Annex II–VI record from the local dataset built from public European Commission cosmetic ingredient materials.

Use this inventory page to research HUMAN NEONATAL FIBROBLAST/KERATINOCYTE CONDITIONED MEDIA and compare linked records, but verify restrictions and legal status against the current official source text and law before making regulatory decisions.

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