ABIES ALBA CONE OIL
Official label name (INCI name, EU glossary of cosmetic ingredient names), No 398
- Allowed with restrictions (Annex III)
ABIES ALBA CONE OIL: Allowed with restrictions (Annex III, entry 103), under Regulation (EC) No 1223/2009.
In plain words
What it is used for
Functions declared by manufacturers:
Perfuming.
What the rules say
Allowed, with restrictions: Annex III sets a warning to be printed on the packaging. Ingredient lists do not give quantities, so the concentration cannot be checked on the label; the warning can.
The text of the annexes
Allowed with restrictions
- Entry
- Annex III, No 103
- Substance
- Abies alba oil and extract
- Glossary names
- ABIES ALBA CONE OIL; ABIES ALBA CONE EXTRACT; ABIES ALBA LEAF OIL; ABIES ALBA LEAF CERA; ABIES ALBA NEEDLE EXTRACT; ABIES ALBA NEEDLE OIL
- CAS
- 90028-76-5
- EC
- 289-870-2
- Other conditions
- Peroxide value less than 10 mmoles/L (15 )
- Warnings
- (15 ) This limit applies to the substance and not to the finished cosmetic product.’
Dates in the act (3)
- Entry into force on 15 May 2013
- Application from 11 July 2013
It shall apply from 11 July 2013.
- Entry into force on 11 July 2013
Excerpts from the English text published in the Official Journal. A date may concern only some substances of the act: the excerpt says so.
Identity
- CosIng identifier
- 41320
- CAS (according to CosIng)
- 90028-76-5
- EC (according to CosIng)
- 289-870-2
- Declared functions
- Perfuming
Name of a plant extract or plant part: its CAS number designates the whole plant, not this ingredient alone.
Elsewhere in the world
Information on other jurisdictions. What is covered, and what is not yet.
United Kingdom (Great Britain)
- Allowed with restrictions (Annex III)
Same entries as in the European Union. Conditions (concentrations, warnings) may differ: they are not compared here.
Switzerland
Regulation (EC) No 1223/2009 applies in Switzerland (Article 54 of the Ordinance on Foodstuffs and Utility Articles).
United States, federal rules
None of the integrated sections of the federal code (21 CFR 700.11 to 700.27 and 250.250) targets this name. The FDA does not publish a list of allowed ingredients.
Glossary: Commission Implementing Decision (EU) 2025/1175. Page updated on 21 October 2026.