NDC 58443-0294 Black Girl Sunscreen Spf 50 Broad Spectrum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 58443-0294?
What are the uses for Black Girl Sunscreen Spf 50 Broad Spectrum?
Which are Black Girl Sunscreen Spf 50 Broad Spectrum UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Black Girl Sunscreen Spf 50 Broad Spectrum 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EDETIC ACID (UNII: 9G34HU7RV0)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARROT SEED OIL (UNII: 595AO13F11)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- JOJOBA OIL (UNII: 724GKU717M)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER 980 (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SHEA BUTTER (UNII: K49155WL9Y)
- CHAMOMILE (UNII: FGL3685T2X)
- BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
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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".