NDC 50051-0011 Tow Mater Sun Smacker Spf 24 Tow-tally Orange
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 50051-0011?
What are the uses for Tow Mater Sun Smacker Spf 24 Tow-tally Orange?
Which are Tow Mater Sun Smacker Spf 24 Tow-tally Orange 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)
- PADIMATE O (UNII: Z11006CMUZ)
- PADIMATE O (UNII: Z11006CMUZ) (Active Moiety)
Which are Tow Mater Sun Smacker Spf 24 Tow-tally Orange 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- CETYL ACETATE (UNII: 4Q43814HXS)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CANDELILLA WAX (UNII: WL0328HX19)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
- SESAME OIL (UNII: QX10HYY4QV)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- BENZYL BENZOATE (UNII: N863NB338G)
- PARAFFIN (UNII: I9O0E3H2ZE)
- WHEAT GERM OIL (UNII: 14C97E680P)
- MICA (UNII: V8A1AW0880)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- NEOTAME (UNII: VJ597D52EX)
- CITRAL (UNII: T7EU0O9VPP)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GERANIOL (UNII: L837108USY)
- METHYL HEPTINE CARBONATE (UNII: 0TTP6YT2T3)
- CINNAMALDEHYDE (UNII: SR60A3XG0F)
- EUGENOL (UNII: 3T8H1794QW)
- FARNESOL (UNII: EB41QIU6JL)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C RED NO. 22 (UNII: 1678RKX8RT)
- D&C RED NO. 6 (UNII: 481744AI4O)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".