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
ALOE VERA LEAF; IMIDUREA; WATER
Active strength
.15; .25; 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

Additional Listing Data#

Finished product
Yes
Brand name base
AnubisMed

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALOE VERA LEAF.15 g/50mL
IMIDUREA.25 g/50mL
WATER45.8293 mL/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZY81Z83H0X, M629807ATL, 059QF0KO0R

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83021-400-50AnubisMed50 mL in 1 BOTTLE, SPRAYLIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83021-400ANUBISMED (SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREA) LIQUID [ANUBIS COSMETICS SL]2Current NDC, Legacy NDC, 1 package rows20230906_ebf4b3ab-34e1-185a-e053-2a95a90ace3a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
83021-400-508302104005050 mL in 1 BOTTLE, SPRAY (83021-400-50) 50 ml2022-10-262027-05-10NoNoCurrent