PERSONAL CARE WET WIPES CITRUS- benzalkonium chloride cloth 
Delta Brands, Inc

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.

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Lucky Wet WipesBzlknmHCl0.13indivpckt

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

for hand sanitizing to decrease bacteria on skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients

When using this product

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues for more than 72 hours

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 years and over ■ apply to hands ■ allow to dry without wiping

children under 2 years ask a doctor before use

Inactive ingredients

water, ethyl alcohol, aloe barbadensis leaf juice, PEG-60 lanolin, fragrance, tetrasodium EDTA, phenoxyethanol, potassium sorbate, quaternium-52, citric acid

Package Label

packet label

PERSONAL CARE WET WIPES  CITRUS
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-436
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
PEG-60 LANOLIN (UNII: K2OI1D27ET)  
QUATERNIUM-52 (UNII: 588EQF3H1P)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
EDETATE SODIUM (UNII: MP1J8420LU)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20276-436-1515 in 1 BOX01/07/2021
1NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
2NDC:20276-436-1818 in 1 BOX01/07/2021
2NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
3NDC:20276-436-3030 in 1 BOX01/07/2021
3NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
4NDC:20276-436-4040 in 1 BOX01/07/2021
4NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/07/2021
Labeler - Delta Brands, Inc (102672008)

Revised: 12/2022
Document Id: eff54541-58b6-1a9c-e053-2995a90a9ac7
Set id: b6c041e5-f61a-4a83-e053-2995a90a15a7
Version: 3
Effective Time: 20221216
 
Delta Brands, Inc