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

Antibacterial

Inactive ingredients

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

Uses

• For hand washing to decrease bacteria on skin

Warnings

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

When using this product

do not use in or near the eyes. In case of contact with eyes, flush thoroughly with water.

Stop use & ask a doctor

if irritation and redness develops and persist for more than 72 hours.

Keep out of reach from children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Take wipe and rub thoroughly over the surface of both hands, then rub hands briskly to dry.
• Dispose after single use.
• Do not flush.

Other information

• Keep away from sunlight. Store at room temperature 20°-25° Celsius (68°-77° Fahrenheit)
• May discolor certain fabrics.

Package Labeling:80 count

ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79021-005
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: 79021-005-80	80 in 1 POUCH	10/15/2020	11/30/2023
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)	10/15/2020	11/30/2023

Labeler - Positive Promotions Inc. (002401719)

Revised: 10/2023

Document Id: 08be3e93-6374-6e37-e063-6294a90a2a6c

34390-5

Set id: b25b91e9-497a-1f80-e053-2a95a90af079

Version: 3

Effective Time: 20231027