NDC 63931-4291 Wl-aab-z-w-330
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 63931-4291?
Which are Wl-aab-z-w-330 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Wl-aab-z-w-330 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ISODODECANE (UNII: A8289P68Y2)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)
- PROPANEDIOL (UNII: 5965N8W85T)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- .BETA.-TOCOPHEROL (UNII: 9U6A490501)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".