WET WIPE- benzalkonium chloride cloth

WET WIPE by

Drug Labeling and Warnings

WET WIPE by is a Otc medication manufactured, distributed, or labeled by JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

WET WIPE

Active Ingredient(s)

Benzalkonium chloride 1mg/pcs. Purpose: Antiseptic

Purpose

Antiseptic, WET WIPE

Use

WET WIPE to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Wipe the surface of the skin and let it dry naturally
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

RO WATER
Sodium Lauryl Sulfate
2-Bromo-2-Nitropropane-1
Glycerin
Aloe Barbadensis Leaf Extract
Vitamin E

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

WET WIPE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69733-101
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
BRONOPOL (UNII: 6PU1E16C9W)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69733-101-01	800 in 1 BAG; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD (421340473)

Establishment
Name	Address	ID/FEI	Business Operations
JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD		421340473	manufacture(69733-101)