Label: BRAVO SIERRA USA FACE SUNSCREEN BROAD SPECTRUM SPF 30 swab
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Contains inactivated NDC Code(s)
NDC Code(s): 73206-020-01 - Packager: ARJOLO, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 16, 2019
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- Active Ingredient
- Purpose
- Use
- Warnings
- Keep out of reach of children
- Directions
- Inactive ingredients
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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 swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73206-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X) BETAINE (UNII: 3SCV180C9W) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) POLYGLYCERYL-6 ISOSTEARATE (UNII: 5VKGO1O03G) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73206-020-01 1 in 1 PACKAGE 07/11/2019 1 5.275 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/11/2019 Labeler - ARJOLO, INC. (117013959)