ANTIBACTERIAL HAND WIPE patch

Antibacterial Hand Wipe by

Drug Labeling and Warnings

Antibacterial Hand Wipe by is a Otc medication manufactured, distributed, or labeled by Fujian Yifa Healthcare Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

Hand sanitizer to help reduce bacteria;
For use when soap and water are not available.

Warnings

For external use only

Do not use

In children less than 2 months old;
On open skin wounds.

When Using

keep out of eyes,ears,and mouth.In case of contact with eyes,rinse eyes thoroughly with water.

Stop Use

If irritation or rash occurs.These may be signs of a serious condition.

Ask 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.

Directions

1.Apply to hands,allow to air dry without wiping;
2.Children under 6 years of age should be supervised when using this product.

Other information

1.Store in a cool,dry place;2.Avoid freezing and excessive heat.

Inactive ingredients

Aloe Barbadensis Leaf Extract,Alpha-Tocopherol,Fragrance,Glycerin,Phenoexyethanol,Propylene Glycol,Water.

Questions

call 718-975-2586

PRINCIPAL DISPLAY PANEL

75543-301-01

PRINCIPAL DISPLAY PANEL

75543-301-02

PRINCIPAL DISPLAY PANEL

75543-301-03

PRINCIPAL DISPLAY PANEL

75543-301-04

PRINCIPAL DISPLAY PANEL

75543-301-05

PRINCIPAL DISPLAY PANEL

75543-301-06

PRINCIPAL DISPLAY PANEL

75543-301-07

PRINCIPAL DISPLAY PANEL

75543-301-08

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND WIPE 
antibacterial hand wipe patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75543-301
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

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75543-301-01	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
2	NDC: 75543-301-02	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
3	NDC: 75543-301-03	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
4	NDC: 75543-301-04	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
5	NDC: 75543-301-05	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
6	NDC: 75543-301-06	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
7	NDC: 75543-301-07	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025
8	NDC: 75543-301-08	40 in 1 PATCH; Type 0: Not a Combination Product	06/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/23/2025

Labeler - Fujian Yifa Healthcare Products Co., Ltd. (420510793)

Establishment
Name	Address	ID/FEI	Business Operations
Fujian Yifa Healthcare Products Co., Ltd.		420510793	manufacture(75543-301)