Label: ANTIBACTERIAL WIPES- benzalkonium chloride swab
- NDC Code(s): 70691-900-13
- Packager: Glaro, Incorporated
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- Adults and Children 2 Years and Over. Apply to hands and face; Allow to dry without wiping.
- Children Under 2 Years: Ask a doctor before use.
To Dispense:
- DO NOT remove wipes roll from the heat sealed plastic bag.
- DO NOT cut across the top of the entire bag.
- Cut a “V” shaped opening on the top center of the bag.
- Pull up the first wipe from the center of the roll.
- Thread through the star shaped opening in the underside of the dispenser cover.
- Secure the cover to the body.
- To dispense, pull each sheet up and slightly to the side.
Dispose of wipes in thrash. Do not flush
- Other information
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70691-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) EDETATE DISODIUM (UNII: 7FLD91C86K) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70691-900-13 2000 in 1 BAG 05/21/2018 1 1 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 Drug M003 05/21/2018 Labeler - Glaro, Incorporated (002048627)