ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

Antibacterial Wet Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

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

Inactive Ingredients

• 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:73796-001-02

Package Labeling:73796-001-04

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73796-001
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: 73796-001-02	15 in 1 BAG	05/15/2020
1		0.006 mL in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 73796-001-04	30 in 1 CONTAINER	05/15/2020
2		0.002 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 not final	part333E	05/15/2020

Labeler - ProStock LLC (078859574)