NDC 73206-010 Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73206-010?
What are the uses for Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30?
Which are Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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 Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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:
- WATER (UNII: 059QF0KO0R)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CAPRYLYL CAPRYLATE (UNII: MM00XO86JQ)
- BIS-ETHYLHEXYL HYDROXYDIMETHOXY BENZYLMALONATE (UNII: 7D4Q5YJ8NV)
- PROPANEDIOL (UNII: 5965N8W85T)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- POLYAMIDE-3 (12000 MW) (UNII: L7P3YWF22X)
- SILICON (UNII: Z4152N8IUI)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SUCROSE (UNII: C151H8M554)
- PANAX QUINQUEFOLIUS WHOLE (UNII: 0P067WOA1X)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TOCOPHEROL (UNII: R0ZB2556P8)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".