NDC 58443-0415 Black Girl Sunscreen Spf 45
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises, Inc.
- 58443-0415 - Black Girl Sunscreen
Product Characteristics
Product Packages
NDC Code 58443-0415-3
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 58443-0415?
What are the uses for Black Girl Sunscreen Spf 45?
Which are Black Girl Sunscreen Spf 45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Black Girl Sunscreen Spf 45 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 ETHYLHEXANOATE (UNII: 134647WMX4)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SHEA BUTTER (UNII: K49155WL9Y)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SQUALANE (UNII: GW89575KF9)
* 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".