NDC 63148-008 Wolf Daily Moisturizier Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63148-008?
What are the uses for Wolf Daily Moisturizier Spf 15?
Which are Wolf Daily Moisturizier Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Wolf Daily Moisturizier Spf 15 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:
- WATER (UNII: 059QF0KO0R)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- LACTIC ACID (UNII: 33X04XA5AT)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL (UNII: 0QW9S92J3K)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PANTHENOL (UNII: WV9CM0O67Z)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- ADANSONIA DIGITATA SEED (UNII: 2936P60TPX)
- TEA TREE OIL (UNII: VIF565UC2G)
- CANNABIS SATIVA SEED (UNII: QE567Z26NG)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- PHYTONADIONE (UNII: A034SE7857)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
* Please review the disclaimer below.
[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".