NDC 62742-4157 Tropical Topical Matte Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4157 - Tropical Topical Matte Spf 30
Product Packages
NDC Code 62742-4157-2
Package Description: 1 TUBE in 1 CARTON / 57 g in 1 TUBE (62742-4157-1)
Product Details
What is NDC 62742-4157?
What are the uses for Tropical Topical Matte Spf 30?
Which are Tropical Topical Matte Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Tropical Topical Matte Spf 30 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)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIEPOXYCYCLOHEXASILANE (UNII: 066Q83563R)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- TEPRENONE (UNII: S8S8451A4O)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)
- PHOENIX DACTYLIFERA WHOLE (UNII: 8QI9RWU9M1)
- POLYGONUM AVICULARE WHOLE (UNII: M990N03611)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- CARBOMER 934 (UNII: Z135WT9208)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".