NDC 55910-418 Skin Corrective Bb Cream Broad Spectrum Spf15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55910 - Dolgencorp Inc.
- 55910-418 - Skin Corrective Bb Cream Broad Spectrum Spf15 Sunscreen
Product Packages
NDC Code 55910-418-11
Package Description: 1 TUBE in 1 CARTON / 75 mL in 1 TUBE
Product Details
What is NDC 55910-418?
What are the uses for Skin Corrective Bb Cream Broad Spectrum Spf15 Sunscreen?
Which are Skin Corrective Bb Cream Broad Spectrum Spf15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Skin Corrective Bb Cream Broad Spectrum Spf15 Sunscreen 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TRICAPRIN (UNII: O1PB8EU98M)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MYRISTATE (UNII: 6992Y81827)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- DOCOSANOL (UNII: 9G1OE216XY)
- MINERAL OIL (UNII: T5L8T28FGP)
- TALC (UNII: 7SEV7J4R1U)
- 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)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- 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".