INTCO HAND SANITIZING WIPES- benzalkonium chloride cloth

INTCO HAND SANITIZING WIPES by

Drug Labeling and Warnings

INTCO HAND SANITIZING WIPES by is a Otc medication manufactured, distributed, or labeled by Jiangsu Intco Medical Products Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient:

Benzalkonium Chloride 0.13%

Purpose

Antiseptic/ hand and skin sanitizer

Uses

Sanitizing hand wipes help decrease bacteria on the skin. Recommended for single use.

Warnings

For external use only

Do not freeze

Do not use

In ears, eyes or mouth

When using this product:

Avoid contact with the eyes

In case of contact, flush eyes with water.

Stop use and ask a doctor if

Redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children

Children should be supervised when using this product.

Directions

Wipe liberally over the hands, rub into skin until dry.

Recommended for single use.

Inactive ingredients

Water, Didecyldimonium Chloride, Phenoxyethanol, Cetylpyridinium Chloride, Aloe Vera Leaf Extract , Tocopherol (Natural Vitamin E), Glycerin, Dimethicone.

INSTRUCTIONS FOR USE

To open package

• Tear open and pull out wipe
• Dispose after use

Dispose

Dispose of wipe in trash after use. Do not flush.

Avoid flushing down the toilet.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INTCO HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74201-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13   in 100

Inactive Ingredients
Ingredient Name	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
WATER (UNII: 059QF0KO0R)
TOCOPHEROL (UNII: R0ZB2556P8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74201-001-01	1 in 1 BAG; Type 0: Not a Combination Product	03/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/12/2021

Labeler - Jiangsu Intco Medical Products Co., Ltd (529128686)