ANTIBACTERIAL HAND WIPES cloth

Antibacterial Hand Wipes by

Drug Labeling and Warnings

Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by GoodFibers. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium

Chloride 0.125%

Purpose

Antimicrobial

USES

*For hand washing to decrease bacteria on skin without requiring water or rinsing.

*Recommended for repeated use

Warnings

For external use only.

When using product

*Do not use in or near eyes.

If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

*If irritation and redness persist for more than 72 hours.

Keep out of reach of children

In case of accidental indestion, seek medical attention or contact a poison control center immediately.

Directions

*Wet thoroughly hands with wipe and allow to dry without wiping.

*Children under six years of age should be supervised when using this product.

Inactive Ingredients

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Citric Acid, Decyl Glucoside, Fragrtance, Phenoxyethanol, Potassium Sorbate, Tetrasodium EDTA, Water.

PDP

MEDIC THERAPEUTICS

ANTIBACTERIAL

HAND WIPES

___________________

KILLS 99.9% OF GERMS

Sanitize on the Go

Active Ingredient -

Benzalkonium Chloride (0.125%)

7 x 5.1in (18 x 13 cm)

20 CT

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND WIPES 
antibacterial hand wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77070-702
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.125 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
EDETATE SODIUM (UNII: MP1J8420LU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77070-702-20	1 g in 1 POUCH; Type 0: Not a Combination Product	07/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/17/2020

Labeler - GoodFibers (105870470)

Registrant - GoodFibers (105870470)

Establishment
Name	Address	ID/FEI	Business Operations
GoodFibers		105870470	manufacture(77070-702)