NDC 11489-094 Botanics Radiant Youth Protecting Day Cream Sunscreen Broad Spectrum Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11489 - Bcm Ltd
- 11489-094 - Botanics Radiant Youth Protecting Day Cream Sunscreen Broad Spectrum Spf 15
Product Packages
NDC Code 11489-094-01
Package Description: 1 JAR in 1 CARTON / 50 g in 1 JAR
Product Details
What is NDC 11489-094?
What are the uses for Botanics Radiant Youth Protecting Day Cream Sunscreen Broad Spectrum Spf 15?
Which are Botanics Radiant Youth Protecting Day Cream Sunscreen Broad Spectrum Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Botanics Radiant Youth Protecting Day Cream Sunscreen Broad Spectrum Spf 15 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- ALMOND OIL (UNII: 66YXD4DKO9)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GINKGO (UNII: 19FUJ2C58T)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- TOCOPHEROL (UNII: R0ZB2556P8)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- TAGETES MINUTA FLOWER OIL (UNII: 1T0ZMU8M8B)
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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".