NDC 76049-201 Stay All Day 10-in-1 Illuminating Skin Veil Broad-spectrum Spf 30 Sunscreen Water-resistant 80 Minutes Kitten Illuminating
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76049-201?
What are the uses for Stay All Day 10-in-1 Illuminating Skin Veil Broad-spectrum Spf 30 Sunscreen Water-resistant 80 Minutes Kitten Illuminating?
Which are Stay All Day 10-in-1 Illuminating Skin Veil Broad-spectrum Spf 30 Sunscreen Water-resistant 80 Minutes Kitten Illuminating UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Stay All Day 10-in-1 Illuminating Skin Veil Broad-spectrum Spf 30 Sunscreen Water-resistant 80 Minutes Kitten Illuminating 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ISODODECANE (UNII: A8289P68Y2)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MICA (UNII: V8A1AW0880)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- APPLE (UNII: B423VGH5S9)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- ALLANTOIN (UNII: 344S277G0Z)
- HEXADECENE (MIXED ISOMERS) (UNII: 38H8547VP0)
- BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
- PEACH (UNII: 3OKE88I3QG)
- TROPAEOLUM MAJUS FLOWERING TOP (UNII: RGT30824HY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".