GOODEARTH SANITIZING WIPES- benzalkonium chloride cloth

GoodEarth Sanitizing Wipes by

Drug Labeling and Warnings

GoodEarth Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by GoodEarth Distribution LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.13 %

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

Use

Hand sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

WARNINGS

Warnings

For external use only.

WHEN USING

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly in water.

STOP USE

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

Keep out of reach of children.

DOSAGE & ADMINISTRATION

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 INGREDIENT

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL

3000 Total Wipes (1500 wipes per roll; 2 rolls per case)

NDC: 71745-003-01

INGREDIENTS AND APPEARANCE

GOODEARTH SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71745-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	3.822 mg

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71745-003-01	2 in 1 CASE	08/11/2023
1		1500 in 1 BAG; 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)	08/11/2023

Labeler - GoodEarth Distribution LLC (079808558)