SANITIZING WIPES- benzalkonium chloride cloth

Sanitizing Wipes by

Drug Labeling and Warnings

Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Guangzhou Baihua Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Sanitizing Wipes

This is a sanitizing wipe product manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product:

1. Benzalkonium Chloride (0.13%)
2. RO pure water
3. Decyl Glucoside (1%)
4. Glycerin (2%)
5. Fragrance (Parfum) (0.03%)
6. Methylparaben (0.1%)
7. Phenoxyethanol (1%)
8. Propylparaben (0.1%)

Active Ingredient(s)

Benzalkonium Chloride 0.13%. Purpose: Antiseptic

Purpose

Antiseptic, Sanitizing Wipes

Use

Sanitizing Wipes to help reduce bacteria on skin. For use when soap and water are not available.

Warnings

For external use only.

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 hands thoroughly with product.
• Supervise children under 6 years of age when using product.

Other information

Inactive ingredients

Water (Aqua), Decyl Glucoside, Glycerin, Fragrance (Parfum), Methylparaben, Phenoxyethanol, Propylparaben

Package Label - Principal Display Panel

100 mL NDC: 77665-102-01

INGREDIENTS AND APPEARANCE

SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77665-102
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 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)	1 g  in 100 g
METHYLPARABEN (UNII: A2I8C7HI9T)	0.1 g  in 100 g
PROPYLPARABEN (UNII: Z8IX2SC1OH)	0.1 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	2 g  in 100 g
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)	1 g  in 100 g
WATER (UNII: 059QF0KO0R)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)	0.03 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77665-102-01	100 g in 1 PACKAGE; Type 0: Not a Combination Product	06/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/18/2020

Labeler - Guangzhou Baihua Co., Ltd (545015588)

Registrant - Guangzhou Baihua Co., Ltd (545015588)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Baihua Co., Ltd		545015588	manufacture(77665-102)