Sombra Cosmetics Inc.
A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.
- Country
- United States
- Registered address
- 5951 OFFICE BLVD. NE, ALBUQUERQUE, New Mexico (NM) 87109, United States (USA)
- Operations here
- labelmanufacture
- FDA identifiers
- FEI 1629960 · DUNS 097464309
Recent inspection flagged official action
FDA classified an inspection here as OAI (official action indicated) within the last two years — the strongest public warning signal a facility gets. This plant is listed on labels for 1 drugs. A supply problem here can ripple to all of them.
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- OAIDrug Quality Assurance2026-05-08
- OAIDrug Quality Assurance2024-07-26
- VAIDrug Quality Assurance2016-08-26
- VAIDrug Quality Assurance2013-07-26
- VAIDrug Quality Assurance2011-06-07
- NAIDrug Quality Assurance2009-07-21
Drugs this plant is listed as making
1 distinct drugs across 1 products name this site in their FDA label.
- MENTHOL and CAMPHORSombra Cosmetics Inc.
Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.