WIPE OUT ANTIBACTERIAL WIPES, FRESH SCENT- benzalkonium chloride cloth

WIPE OUT Antibacterial Wipes, Fresh Scent by

Drug Labeling and Warnings

WIPE OUT Antibacterial Wipes, Fresh Scent by is a Otc medication manufactured, distributed, or labeled by Jianerkang Medical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

To decrease bacteria on the skin that could cause disease

Warnings

• For external use only

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin

Stop use and ask a doctor if

• irritation and redness develops
• condition persists 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

• allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other Information

• keep containers tightly closed in a dry, cool and well-ventilated place.
• recommended storage temperature: 32°F to 104°F (0°C to 40°C)

Inactive Ingredients

aloe barbadensis leaf juice, fragrance, phenoxyethanol, polysorbate 20, propylene glycol, tocopheryl acetate, water

Package Labeling:20 count

Package Labeling:80 count

INGREDIENTS AND APPEARANCE

WIPE OUT ANTIBACTERIAL WIPES, FRESH SCENT 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 34645-0010
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 34645-0010-1	20 in 1 BAG	09/12/2020
1		4.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 34645-0010-2	80 in 1 BOTTLE	09/12/2020
2		3.525 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/12/2020

Labeler - Jianerkang Medical Co., Ltd (530968767)