NDC 51702-114 Sun Defeated Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51702-114?
What are the uses for Sun Defeated Sunscreen?
Which are Sun Defeated Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Sun Defeated 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SORBITOL (UNII: 506T60A25R)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- CUCUMBER JUICE (UNII: 61845009SP)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- ARNICA MONTANA (UNII: O80TY208ZW)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETIC ACID (UNII: 9G34HU7RV0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
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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".