NDC 76354-863 Bb Cream Spf 20 Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76354 - J. A. Cosmetics U.s. Inc
- 76354-863 - Bb Cream Spf 20 Beige
Product Packages
NDC Code 76354-863-01
Package Description: 28.5 mL in 1 BOTTLE
Product Details
What is NDC 76354-863?
What are the uses for Bb Cream Spf 20 Beige?
Which are Bb Cream Spf 20 Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Bb Cream Spf 20 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENTOQUATAM (UNII: 7F465U79Q1)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ZINC STEARATE (UNII: H92E6QA4FV)
- TALC (UNII: 7SEV7J4R1U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- JOJOBA OIL (UNII: 724GKU717M)
- CUCUMBER (UNII: YY7C30VXJT)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- LEVOMENOL (UNII: 24WE03BX2T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
* Please review the disclaimer below.
[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".