NDC 47993-216 Sunscreen Spf30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 47993-216?
What are the uses for Sunscreen Spf30?
Which are Sunscreen Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PEG-100 STEARATE (UNII: YD01N1999R)
- PEG-100 STEARATE (UNII: YD01N1999R) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) (Active Moiety)
- BENZOPHENONE (UNII: 701M4TTV9O)
- BENZOPHENONE (UNII: 701M4TTV9O) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Sunscreen Spf30 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- SILICON (UNII: Z4152N8IUI)
- 4-HYDROXYBENZOIC ACID (UNII: JG8Z55Y12H)
- PROPYL ACETATE (UNII: 4AWM8C91G6)
- GLYCERYL MONOOLEATE CITRATE (UNII: NLE5KIG74K)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ETHYLENE GLYCOL (UNII: FC72KVT52F)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2-BUTANEDIOL (UNII: RUN0H01QEU)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".