Label: REMEVERSE INSTANT FOAM HAND SANITIZER- benzalkonium chloride liquid
- NDC Code(s): 70317-145-30
- Packager: RemeVerse
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- RemeVerse instant foam hand sanitizer
- RemeVerse Instant Foam Hand Sanitizer
- Topical Antimicrobial
- Benzalkonium Chloride .1% Active
- Warnings:
- Safety Warning
- Warning - Children
- Purpose - Antimicrobial
- Label
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INGREDIENTS AND APPEARANCE
REMEVERSE INSTANT FOAM HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70317-145 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 300 mL Inactive Ingredients Ingredient Name Strength DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) 0.1 g in 300 mL ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.1 g in 300 mL FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 0.1 g in 300 mL CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) 0.1 g in 300 mL COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) 0.1 g in 300 mL Product Characteristics Color Score Shape ROUND Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70317-145-30 300 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 03/31/2020 Labeler - RemeVerse (050186540) Registrant - Lexia LLC (015552120) Establishment Name Address ID/FEI Business Operations Lexia, LLC 015552120 manufacture(70317-145)