NDC 98132-762 Buxom Show Some Skin Weightless Foundation Broad Spectrum Spf 30 Silky Negli-beige
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 98132-762?
What are the uses for Buxom Show Some Skin Weightless Foundation Broad Spectrum Spf 30 Silky Negli-beige?
Which are Buxom Show Some Skin Weightless Foundation Broad Spectrum Spf 30 Silky Negli-beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Buxom Show Some Skin Weightless Foundation Broad Spectrum Spf 30 Silky Negli-beige 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 (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIETHYLHEXYL SUCCINATE (UNII: 69W9UMG3P8)
- GLYCERIN (UNII: PDC6A3C0OX)
- NYLON-12 (UNII: 446U8J075B)
- PROPANEDIOL (UNII: 5965N8W85T)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
- TAMARIND SEED (UNII: 6AHP8A7OML)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- TALC (UNII: 7SEV7J4R1U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SEA SALT (UNII: 87GE52P74G)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- TURMERIC (UNII: 856YO1Z64F)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".