NDC 68828-131 Daily Defense Spf 15 Jafra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68828 - Jafra Cosmetics International Inc
- 68828-131 - Daily Defense Spf 15
Product Packages
NDC Code 68828-131-02
Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR (68828-131-01)
Product Details
What is NDC 68828-131?
What are the uses for Daily Defense Spf 15 Jafra?
Which are Daily Defense Spf 15 Jafra UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Daily Defense Spf 15 Jafra 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)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TRIDECYL NEOPENTANOATE (UNII: 3Z8H1DA7J5)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- WHEAT GERM (UNII: YR3G369F5A)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- CERAMIDE 3 (UNII: 4370DF050B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PANTHENOL (UNII: WV9CM0O67Z)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBYL METHYLSILANOL PECTINATE (UNII: M3PF9237YC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- 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".