Home NDC 83021-501 Anubis Barcelona
Product NDC 83021-501
11-digit product format 830210501
Labeler code 83021
Product ID 83021-501_04529ef6-e35b-95c2-e063-6394a90ae70d
Type HUMAN OTC DRUG
Nonproprietary name Ferulic Acid, Vitamin C, DMAE
Dosage form CONCENTRATE
Route TOPICAL
Labeler ANUBIS COSMETICS SL
Application M016
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-10-13
Marketing end 2028-01-24
Substance ALCOHOL; GLYCERIN; LECITHIN, SOYBEAN; WATER; MALONDIALDEHYDE; POLYOXYL 35 CASTOR OIL; FRAGRANCE 13576; PEG-8 CAPRYLIC/CAPRIC GLYCERIDES; FERULIC ACID
Active strength .96; .02; .12; 14.26; 2; .18; .02; 2; .1 mL/20mL; g/20mL; g/20mL; mL/20mL; g/20mL; g/20mL; g/20mL; g/20mL; g/20mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Anubis Barcelona Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .96 mL/20mL GLYCERIN .02 g/20mL LECITHIN, SOYBEAN .12 g/20mL WATER 14.26 mL/20mL MALONDIALDEHYDE 2 g/20mL POLYOXYL 35 CASTOR OIL .18 g/20mL FRAGRANCE 13576 .02 g/20mL PEG-8 CAPRYLIC/CAPRIC GLYCERIDES 2 g/20mL FERULIC ACID .1 g/20mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83021-501-20 Anubis Barcelona 20 mL in 1 BOTTLE, DROPPER CONCENTRATE 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83021-501 ANUBIS BARCELONA (FERULIC ACID, VITAMIN C, DMAE) CONCENTRATE [ANUBIS COSMETICS SL] 2 Current NDC, Legacy NDC, 1 package rows 20230902_eaf0770c-795d-0232-e053-2a95a90ae0b5.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 59 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 83021-501-20 83021050120 20 mL in 1 BOTTLE, DROPPER (83021-501-20) 20 ml 2022-10-13 2028-01-24 No No Current