SANITIZING WIPES ALCOHOL FREE FRAGRANCE FREE- benzalkonium chloride cloth

Sanitizing Wipes by

Drug Labeling and Warnings

Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by GoodEarth Distribution Llc, Innocore Sales & Marketing Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13 %

Purpose

Antimicrobal

Use

Hand sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

If swallowed get medical help or contact a poison control center immediately.

Keep out of reach of children.

Directions

• Wet hands thoroughly with product and allow to dry.
• Be sure to use entire wipe.
• Discard after single use.
• Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

Questions

Questions? 1-201-363-1900

PRINCIPAL DISPLAY PANEL

GoodEarth

Sanitizing Wipes

ALCOHOL FREE

FRAGRANCE FREE

Kills 99.99% of most common

germs that may cause illness

Premium fabric quickly removes dirt and soil

Contains 1800 sheets

8" x 5"

To open package:

1 Cut open top

of bag and

remove

plastic tube.

2 Locate wipe at

center of roll.

Do not pull wipe

from side of roll.

3 Insert corner of

wipe through

opening in

dispenser. Next

sheet pops up

automatically.

MADE IN CANADA
Manufactured for and Distributed by:
GoodEarth Distribution LLC
CS@GoodEarthProducts.com
+1-201-363-1900
www.GoodEarthProducts.com

Do Good. Be Good. TM

GoodEarth

INGREDIENTS AND APPEARANCE

SANITIZING WIPES  ALCOHOL FREE FRAGRANCE FREE
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71745-002
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71745-002-02	2 in 1 BOX	01/01/2022
1	NDC: 71745-002-01	1800 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2022

Labeler - GoodEarth Distribution Llc (079808558)

Registrant - Innocore Sales & Marketing Inc (201152597)