Home NDC 83021-400 AnubisMed
Product NDC 83021-400
11-digit product format 830210400
Labeler code 83021
Product ID 83021-400_049fe4c2-996a-198f-e063-6294a90a40b9
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea
Dosage form LIQUID
Route TOPICAL
Labeler ANUBIS COSMETICS SL
Application M016
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-10-26
Marketing end 2027-05-10
Substance IMIDUREA; ALOE VERA LEAF; WATER
Active strength .25; .15; 45.8293 g/50mL; g/50mL; mL/50mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], 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 AnubisMed Active Ingredients# Ingredient, Strength table Ingredient Strength IMIDUREA .25 g/50mL ALOE VERA LEAF .15 g/50mL WATER 45.8293 mL/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination M629807ATL Internal UNII lookup ZY81Z83H0X Internal UNII lookup 059QF0KO0R Internal UNII lookup
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 83021-400-50 AnubisMed 50 mL in 1 BOTTLE, SPRAY LIQUID 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83021-400 ANUBISMED (SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREA) LIQUID [ANUBIS COSMETICS SL] 2 Current NDC, Legacy NDC, 1 package rows 20230906_ebf4b3ab-34e1-185a-e053-2a95a90ace3a.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 53 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 83021-400-50 83021040050 50 mL in 1 BOTTLE, SPRAY (83021-400-50) 50 ml 2022-10-26 2027-05-10 No No Current