NDC 75391-002 Sea Starwort Soothing Sunscreen Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75391 - Cu Lifestyle Llc
- 75391-002 - Sea Starwort Soothing Sunscreen Spf 35
Product Characteristics
Product Packages
NDC Code 75391-002-30
Package Description: 30 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 75391-002?
Which are Sea Starwort Soothing Sunscreen Spf 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sea Starwort Soothing Sunscreen Spf 35 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- WATER (UNII: 059QF0KO0R)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- XANTHAN GUM (UNII: TTV12P4NEE)
- APPLE FRUIT OIL (UNII: 9NT987I3A8)
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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".