NDC 75936-139 Forever Young Body Butter Broad Spectrum Sunscreen Spf 40 Supergoop
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75936-139?
What are the uses for Forever Young Body Butter Broad Spectrum Sunscreen Spf 40 Supergoop?
Which are Forever Young Body Butter Broad Spectrum Sunscreen Spf 40 Supergoop UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Forever Young Body Butter Broad Spectrum Sunscreen Spf 40 Supergoop 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)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- APPLE (UNII: B423VGH5S9)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- STARCH, CORN (UNII: O8232NY3SJ)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MANDARIN OIL (UNII: NJO720F72R)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- CARDAMOM OIL (UNII: JM0KJ091HZ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- CLOVE OIL (UNII: 578389D6D0)
- LAVANDIN OIL (UNII: 9RES347CKG)
- VANILLA (UNII: Q74T35078H)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PURSLANE (UNII: M6S840WXG5)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TOCOPHEROL (UNII: R0ZB2556P8)
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[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".