Home NDC 83021-750 ANUBISMED
Product NDC 83021-750
11-digit product format 830210750
Labeler code 83021
Product ID 83021-750_049f9ce0-73cc-2865-e063-6394a90a505a
Type HUMAN OTC DRUG
Nonproprietary name HA HYALURONIC
Dosage form CREAM
Route TOPICAL
Labeler ANUBIS COSMETICS SL
Application M016
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-10-17
Marketing end 2028-01-16
Substance ALLANTOIN; ALOE VERA LEAF; FRAGRANCE 13576; GLYCERYL MONOSTEARATE; TROLAMINE; BUTYLATED HYDROXYTOLUENE; PROPYLENE GLYCOL; CETYL ALCOHOL; TROPOLONE; TOCOPHEROL; DIMETHICONE; 1,2-HEXANEDIOL; IMIDUREA; CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE; CETEARYL ETHYLHEXANOATE; MEDIUM-CHAIN TRIGLYCERIDES; CAPRYLYL GLYCOL; OCTINOXATE; GLYCERIN; GLYCERYL STEARATE SE; WATER; C12-20 ACID PEG-8 ESTER; OXYBENZONE; DECYL OLEATE
Active strength .05; 2.5; .225; .875; .3; .0535; 1.996; .0038; .004; .0004; .25; .198; .15; .25; 1.75; 1.5; .198; 3.4965; .4975; 1.5; 27.4065; 2.25; 2; 1.9996 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; mL/50mL; g/50mL; g/50mL; g/50mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], Skin Barrier Activity [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 ALLANTOIN .05 g/50mL ALOE VERA LEAF 2.5 g/50mL FRAGRANCE 13576 .225 g/50mL GLYCERYL MONOSTEARATE .875 g/50mL TROLAMINE .3 g/50mL BUTYLATED HYDROXYTOLUENE .0535 g/50mL PROPYLENE GLYCOL 1.996 g/50mL CETYL ALCOHOL .0038 g/50mL TROPOLONE .004 g/50mL TOCOPHEROL .0004 g/50mL DIMETHICONE .25 g/50mL 1,2-HEXANEDIOL .198 g/50mL IMIDUREA .15 g/50mL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE .25 g/50mL CETEARYL ETHYLHEXANOATE 1.75 g/50mL MEDIUM-CHAIN TRIGLYCERIDES 1.5 g/50mL CAPRYLYL GLYCOL .198 g/50mL OCTINOXATE 3.4965 g/50mL GLYCERIN .4975 g/50mL GLYCERYL STEARATE SE 1.5 g/50mL WATER 27.4065 mL/50mL C12-20 ACID PEG-8 ESTER 2.25 g/50mL OXYBENZONE 2 g/50mL DECYL OLEATE 1.9996 g/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 24 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 83021-750-50 ANUBISMED 50 mL in 1 JAR CREAM 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83021-750 ANUBISMED (HA HYALURONIC) CREAM [ANUBIS COSMETICS SL] 2 Current NDC, Legacy NDC, 1 package rows 20230906_eac771e2-4c1b-3808-e053-2995a90ac5fc.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 38 of 68 · 1,350 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 83021-750-50 83021075050 50 mL in 1 JAR (83021-750-50) 50 ml 2022-10-17 2028-01-16 No No Current