Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial agent

Decreases bacteria on skin.

For external use only.

Do not use if you are allergic to any of the ingredients.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Open lid and remove wipes.
Wet hands thoroughly with product and let hands air dry.
Throw used wipe in trash.
Do not flush.


Adults and children 2 years and over:	Apply to hands. allow hands to dry without wiping.
Children under 2 years:	Ask a doctor before use.

c12-14 Alkyl Dymethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene glycol, Aqua

Label, 10 Wipes

Label_1

Label 110 Wipes
Label_2

GREENBERRY
benzalkonium cloth

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) (UNII: 85440928RV)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:77965-001-01	10 in 1 POUCH	06/10/2020
1		3.8 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
2	NDC:77965-001-02	72 in 1 CANISTER	06/10/2020
2		3.8 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
3	NDC:77965-001-03	110 in 1 POUCH	06/10/2020
3		3.8 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/10/2020

Labeler - Greenberry Eco Group LLC (080300128)