MOXIE HAND WIPES- benzalkonium chloride cloth 
Skaffles Group

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Moxie Antibacterial Hand Wipes


Active Ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antibacterial

DRUG FACTS

Use

Warnings

For external use only.

Do not use

Discontinue use if irritation and redness develop.If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive Ingredients

Water, Phenoxyethanol, Potassium Sorbate, Sodum Benzoate, Cetylpyridinium Chloride, Disodium Cocoamphodiacetate, Disodium EDTA, PEG-8 Dimethicone, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricacria), Flower Extract, Quaternium-52, Citric Acid, PEG075 Lanolin.

888-251-009

Principal Display Panel

Moxie

ANTIBACTERIAL HAND WIPES

Kills 99.9% of most comon gems

Moisturizes with Aloe

Unscented

6.5 in x 4.5 in (16.5 cm x 11.4 cm)

1CT

Distributed by: Lowe's Home Centers LLC,

Mooresville NC 28117 888-251-009

MADE IN CHINA

See outer packaging for manufacturing date & expiration date

Principal DP

MOXIE HAND WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77720-035
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
PEG-75 LANOLIN (UNII: 09179OX7TB)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
QUATERNIUM-52 (UNII: 588EQF3H1P)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
WATER (UNII: 059QF0KO0R)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Product Characteristics
Color    Score    
ShapeRECTANGLESize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77720-035-011 mL in 1 POUCH; Type 0: Not a Combination Product05/06/2024
2NDC:77720-035-0250 mL in 1 POUCH; Type 0: Not a Combination Product05/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/06/2024
Labeler - Skaffles Group (831115642)

Revised: 5/2024
Document Id: 1887c2ef-b83b-5482-e063-6394a90a00eb
Set id: 17cd6c1a-7b31-3975-e063-6294a90a41c5
Version: 2
Effective Time: 20240515
 
Skaffles Group