Antibacterial Wet Wipes by Positive Promotions Inc. Antibacterial Wet Wipes

Antibacterial Wet Wipes by

Drug Labeling and Warnings

Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Positive Promotions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth 
Positive Promotions Inc.

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Antibacterial Wet Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic

Uses

• For hand-washing to decrease bacteria on skin

Warnings

Flammable. Keep away from heat and flame.For External use only.

Do not use

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach from children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

• Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
• Thoroughly wipe hands, allow to dry out rinsing.
• Discard after single use

Other information

• Do not flush down toilet.
• Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
• May discolor certain fabrics

Inactive Ingredients

Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Aloe Barbadensis Leaf Juice, Sodium Citrate

Package Labeling:15 count

ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79021-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79021-003-15	15 in 1 POUCH	10/01/2020	12/31/2023
1		1.5 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/01/2020	12/31/2023

Labeler - Positive Promotions Inc. (002401719)

Revised: 1/2024

Document Id: 08be3a9f-6760-d317-e063-6394a90a8fb1

34390-5

Set id: af487a42-0c8d-0090-e053-2a95a90afb50

Version: 4

Effective Time: 20240126