NDC 50051-0005 Goofy Sun Smacker Spf 24 Berry Goal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50051 - Bonne Bell Llc
- 50051-0005 - Goofy Sun Smacker Spf 24 Berry Goal
Product Characteristics
Product Packages
NDC Code 50051-0005-4
Package Description: 4 g in 1 CYLINDER
Product Details
What is NDC 50051-0005?
What are the uses for Goofy Sun Smacker Spf 24 Berry Goal?
Which are Goofy Sun Smacker Spf 24 Berry Goal 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 Goofy Sun Smacker Spf 24 Berry Goal 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)
* Please review the disclaimer below.
[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".