Label: ANTIBACTERIAL HAND WIPES (0.13% BENZALKONIUM CHLORIDE)- benzalkonium chloride cloth
- NDC Code(s): 79747-013-20
- Packager: Eleeo Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 25, 2026
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- DO NOT USE
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children
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Directions
- Rub wipe over all surfaces of both hands. Wet hands thoroughly with wipe.
- Allow to dry without wiping
- Children under 2 years of age: ask doctor prior to use
- Children under 6 years of age: use adult supervision
TO USE: Peel back the front label and remove wipe. Firmly reseal the label to close. Dispense of used wipes in the teash. DO NOT FLUSH.
- Other information
- Inactive ingredients
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Package label. Principal display panel
NDC 79747-013-20
Boogie Antibacterial Hand Wipes
Wipe away dirt, messes and bacteria
Moisturizing and gentle
Hypoallergic
Boogie Antibacterial Hand Wipes wipe away dirt, messess and bacteria from hands when soap and water are not available. Other hand wipes contain ethyl alcohol which can be drying and harsh on skin. Our formula is free of drying alcohols, hypoallergenic and made with aloe and Vitamin E to moisturize skin.

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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND WIPES (0.13% BENZALKONIUM CHLORIDE)
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79747-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 5.2 mg Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) CITRIC ACID (UNII: 2968PHW8QP) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM BENZOATE (UNII: OJ245FE5EU) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79747-013-20 20 in 1 PACKET 06/29/2026 1 5.2 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 M004 07/27/2020 Labeler - Eleeo Brands LLC (078476782) Registrant - Precare Corp (858442403)
