Label: BRAVO SIERRA USA FACE SUNSCREEN BROAD SPECTRUM SPF 30 lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 73206-010-03 - Packager: ARJOLO, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 6, 2019
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- Active Ingredients
- Uses
- Warnings
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Directions
• apply generously 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water-resistant sunscreen if swimming or sweating
• Sun Protection Measures. Spending time in the sun
increases your risk of skin cancer and early skin aging. To decrease
this risk, regularly use a sunscreen with a Broad Spectrum SPF
value of 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor -
Inactive ingredients
Water/Aqua/Eau, Butyloctyl Salicylate, Dipropylene Glycol, Caprylyl Methicone, Bis-Ethylhexyl Hydroxydimethoxy Benzylmalonate, Propanediol, Hydrogenated Polyisobutene, Acrylates Copolymer, Methyl Dihydroabietate, Ammonium Acry loyldimethyltaurate/P Copolymer, Polyamide-1, Silica, Glycerin, Tocopheryl Acetate, Saccharide Isomerate, Disodium EDTA, Dipotassium Glycyrrhizate, Sodium Hydroxide, Aloe Barbadensis Leaf Juice, Sucrose, Panax Quinquefolius Root Extract, Plankton Extract, Lecithin, Benzyl Alcohol, Ethylhexylglycerin, Tocopherol
- Other Information
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INGREDIENTS AND APPEARANCE
BRAVO SIERRA USA FACE SUNSCREEN BROAD SPECTRUM SPF 30
bravo sierra usa face sunscreen broad spectrum spf 30 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73206-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73206-010-03 1 in 1 CARTON 07/06/2019 1 3 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 07/06/2019 Labeler - ARJOLO, INC. (117013959)
