Sanitizing Wipes Alcohol Free Fragrance Free: Package Insert and Label Information

SANITIZING WIPES ALCOHOL FREE FRAGRANCE FREE- benzalkonium chloride cloth
GoodEarth Distribution Llc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

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 DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg

Inactive Ingredients Ingredient Name Strength WATER PROPYLENE GLYCOL CAPRYLYL/CAPRYL OLIGOGLUCOSIDE POLY(LAURYLGLUCOSIDE)-7 PHENOXYETHANOL BENZOIC ACID DEHYDROACETIC ACID

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:71745-002-02 2 POUCH in 1 BOX contains a POUCH (71745-002-01) 1 NDC:71745-002-01 1800 CLOTH in 1 POUCH This package is contained within the BOX (71745-002-02)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2022

Labeler — GoodEarth Distribution Llc (079808558)

Registrant — Innocore Sales & Marketing Inc (201152597)

Revised: 01/2022 GoodEarth Distribution Llc