NDC 76169-101 Renewing Antioxidant Treatment Spf 6 Gnld International
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76169 - Gnld International
- 76169-101 - Renewing Antioxidant Treatment Spf 6
Product Packages
NDC Code 76169-101-02
Package Description: 1 JAR in 1 BOX / 50 g in 1 JAR (76169-101-01)
Product Details
What is NDC 76169-101?
What are the uses for Renewing Antioxidant Treatment Spf 6 Gnld International?
Which are Renewing Antioxidant Treatment Spf 6 Gnld International UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Renewing Antioxidant Treatment Spf 6 Gnld International 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)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DECYL OLEATE (UNII: ZGR06DO97T)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- SHEANUT OIL (UNII: O88E196QRF)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PEANUT OIL (UNII: 5TL50QU0W4)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- CETEARETH-15 (UNII: 867H4YOZ8Z)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETEARETH-25 (UNII: 8FA93U5T67)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PEG-30 STEARATE (UNII: 1U8KB35S20)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".