NDC 72344-008 Surface Sun Sheer Touch Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72344-008?
What are the uses for Surface Sun Sheer Touch Spf 30 Sunscreen?
Which are Surface Sun Sheer Touch Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Surface Sun Sheer Touch Spf 30 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:
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ACRYLIC ACID (UNII: J94PBK7X8S)
- TRIMETHYLSILOXYSILICATE (M/Q 0.66) (UNII: 5041RX63GN)
- EDETIC ACID (UNII: 9G34HU7RV0)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
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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".