NDC 73517-125 Squalane Zinc Sheer Mineral Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73517 - Amyris, Inc
- 73517-125 - Squalane Zinc Sheer Mineral Sunscreen
Product Packages
NDC Code 73517-125-01
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 73517-125?
What are the uses for Squalane Zinc Sheer Mineral Sunscreen?
Which are Squalane Zinc Sheer Mineral Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Squalane Zinc Sheer Mineral Sunscreen 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- COCO GLUCOSIDE (UNII: ICS790225B)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- SQUALANE (UNII: GW89575KF9)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYL FERULATE (UNII: 5B8915UELW)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ACACIA (UNII: 5C5403N26O)
- WATER (UNII: 059QF0KO0R)
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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".