NDC 70367-006 Broad Spectrum Moisturizing Sunscreen-spf 15, Octinoxate, Oxybenzone
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Product Details
What is NDC 70367-006?
What are the uses for Broad Spectrum Moisturizing Sunscreen-spf 15, Octinoxate, Oxybenzone?
Which are Broad Spectrum Moisturizing Sunscreen-spf 15, Octinoxate, Oxybenzone UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Broad Spectrum Moisturizing Sunscreen-spf 15, Octinoxate, Oxybenzone 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- SQUALANE (UNII: GW89575KF9)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- ALLANTOIN (UNII: 344S277G0Z)
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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".