NDC 72688-107 Project Sunscreen Spfu Mineral Sunscreen Roll-on Spf-50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72688 - Project Sunscreen
- 72688-107 - Project Sunscreen Spfu Mineral Sunscreen Roll-on
Product Packages
NDC Code 72688-107-11
Package Description: 85 g in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 72688-107?
What are the uses for Project Sunscreen Spfu Mineral Sunscreen Roll-on Spf-50?
Which are Project Sunscreen Spfu Mineral Sunscreen Roll-on Spf-50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Project Sunscreen Spfu Mineral Sunscreen Roll-on Spf-50 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".