NDC 62742-4099 Mineral Foundation Spf 30-5w
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62742-4099?
What are the uses for Mineral Foundation Spf 30-5w?
Which are Mineral Foundation Spf 30-5w UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Mineral Foundation Spf 30-5w 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:
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- PERFLUNAFENE (UNII: 54A06VV62N)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- NYLON-12 (UNII: 446U8J075B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SANDALWOOD (UNII: 3641YW25N2)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- BARLEY (UNII: 5PWM7YLI7R)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
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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".