SANITIZING WET WIPES- alkyl dimethyl benzyl ammonium chloride cloth

Sanitizing Wet Wipes by

Drug Labeling and Warnings

Sanitizing Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Jiangsu Xiaolikang Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Sanitizing Wet Wipes

Active Ingredient(s)

Alkyl dimethyl benzyl ammonium chloride, 0.224mg/pcs
Dioctyl dimethyl ammonium chloride, 0.168mg/pcs
Didecyl dimethyl ammonium chloride, 0.07mg/pcs
Octyl decyl dimethyl ammonium chloride, 0.1mg/pcs

Purpose

Antiseptic, Sanitizing Wet Wipes

Use

Sanitizing Wet Wipes 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 air dry
• 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

Glycerin
2-Bromo-2-Nitropropane-1
IPBC
PHMB(Polyaminopropyl Biguanide)
Aloe Barbadensis Leaf Extract
Vitamin E

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SANITIZING WET WIPES 
alkyl dimethyl benzyl ammonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80337-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUATERNIUM-24 (UNII: 0T2NG1539G) (QUATERNIUM-24 - UNII:0T2NG1539G)	QUATERNIUM-24	0.1 mg
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.224 mg
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.07 mg

Inactive Ingredients
Ingredient Name	Strength
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
GLYCERIN (UNII: PDC6A3C0OX)
DIOCTYLDIMONIUM CHLORIDE (UNII: 0X0RL40Y6H)	0.168 mg
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
BRONOPOL (UNII: 6PU1E16C9W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80337-201-01	80 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
unapproved drug other		03/30/2020

Labeler - Jiangsu Xiaolikang Medical Technology Co., Ltd. (554546867)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangsu Xiaolikang Medical Technology Co., Ltd.		554546867	manufacture(80337-201)