NDC 63868-253 Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Medium Dark
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Chain Drug Marketing Association
- 63868-253 - Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Medium Dark
Product Packages
NDC Code 63868-253-03
Package Description: 1 TUBE in 1 CARTON / 75 mL in 1 TUBE
Product Details
What is NDC 63868-253?
What are the uses for Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Medium Dark?
Which are Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Medium Dark UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Medium Dark 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)
- TALC (UNII: 7SEV7J4R1U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MYRISTATE (UNII: 6992Y81827)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- DOCOSANOL (UNII: 9G1OE216XY)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- FERROUS OXIDE (UNII: G7036X8B5H)
- NYLON-12 (UNII: 446U8J075B)
- TROLAMINE (UNII: 9O3K93S3TK)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALLANTOIN (UNII: 344S277G0Z)
- CAFFEINE (UNII: 3G6A5W338E)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HYALURONIC ACID (UNII: S270N0TRQY)
* 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".