Label: WET ONES- benzalkonium chloride swab
- NDC Code(s): 63354-774-14, 63354-774-20, 63354-774-24, 63354-774-40
- Packager: Edgewell Personal Care Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 24, 2024
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- Active Ingredient
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- Inactive Ingredients
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Principal Display Panel
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Fresh Scent
Kills 99.99% of Germs*
Hypoallergenic
WET LOCK SEAL
Keeps Wipes Moist
LIFT HERETough on Germs
Gentle on Skin
20
wipes
Do Not FlushTEAR HERE
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Fresh Scent
Kills 99.99% of Germs*
Hypoallergenic
*Effective at killing 99.99% of many
common harmful bacteria in as little
as 15 seconds
1 wipeTEAR HERE
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Fresh Scent
Kills 99.99% of Germs*
Hypoallergenic
*Effective at killing 99.99% of many
common harmful bacteria in as little
as 15 seconds
1 wipe
actual sizePocket Size
Singles
Tough on Germs
Gentle on Skin
Hypoallergenic
Paraben Free
America’s
#1 Hand Wipe*
24 INDIVIDUALLY
WRAPPED WIPESWet
Ones
ANTIBACTERIAL
HAND WIPE
Fresh Scent
Kills 99.99% of Germs*
Tough on Germs
Gentle on Skin
Hypoallergenic
Do Not Flush
40
wipesTough on Germs
Gentle on Skin
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Fresh Scent
Kills 99.99% of Germs*
Hypoallergenic
WET LOCK SEAL
Keeps Wipes Moist
LIFT HERE
20
wipes
Do Not Flush7 - 20ct. TRAVEL PACKS
140 TOTAL WIPES
Wet
Ones
ANTIBACTERIAL
HAND WIPE
7 Travel
Packs
Kills 99.99% of Germs* -
INGREDIENTS AND APPEARANCE
WET ONES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-774 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-8 DIMETHICONE (UNII: GIA7T764OD) EDETATE DISODIUM (UNII: 7FLD91C86K) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-774-20 20 in 1 POUCH; Type 0: Not a Combination Product 09/17/2024 2 NDC:63354-774-24 24 in 1 PACKET; Type 0: Not a Combination Product 09/17/2024 3 NDC:63354-774-40 40 in 1 CANISTER; Type 0: Not a Combination Product 09/17/2024 4 NDC:63354-774-14 140 in 1 PACKET; Type 0: Not a Combination Product 09/17/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 09/17/2024 Labeler - Edgewell Personal Care Brands LLC (151179769)