PPE Advantage Wet Wipes by Zhejiang iColor Biotech Co., Ltd PPE Advantage Wet Wipes

PPE Advantage Wet Wipes by

Drug Labeling and Warnings

PPE Advantage Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PPE ADVANTAGE WET WIPES- benzalkonium chloride gel 
Zhejiang iColor Biotech Co., Ltd

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PPE Advantage Wet Wipes

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses

• Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only

When using this product

do not use in or near 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 appears on the skin.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

• Wet hands thoroughly with product and allow to dry.
• Discard wipe in trash receptacle after use. Do not flush.
• Children under 6 years of age should be supervised by adult when applying this product.

Inactive ingredients

Ethylhexylglycerin, Glycerin, Phenoxyethanol, Polyaminopropyl biguanide, Propylene Glycol, Purified water, Fragrance

Questions or Comments?

212-551-2657

Package Labeling:100ct

Package Labeling:220ct

PPE ADVANTAGE WET WIPES 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-046
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  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-046-01	100 in 1 CANISTER	08/10/2020	01/31/2026
1		4.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 74934-046-02	220 in 1 CANISTER	08/10/2020	01/31/2026
2		4.2 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)	08/10/2020	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)

Revised: 1/2024

Document Id: 0fb27dc1-dce6-13a9-e063-6394a90acaec

34390-5

Set id: 1ed15c2a-f70e-4dc2-a1f5-414345ff1a6b

Version: 2

Effective Time: 20240124