FRAGRANCE FREE SANITIZING WIPES- benzalkonium chloride cloth

Fragrance Free Sanitizing Wipes by

Drug Labeling and Warnings

Fragrance Free 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

Water, propylene glycol, decyl/lauryl glucoside, phenoxyethanol, benzoic acid, dehydroacetic acid.

PRINCIPAL DISPLAY PANEL - 1800 Count Pouch Label

GoodEarth
DISTRIBUTION

FRAGRANCE FREE

Kills 99.99%
of most common germs
that may cause illness

Sanitizing
wipes

1800
count

Premium fabric quickly
removes dirt and soil

INGREDIENTS AND APPEARANCE

FRAGRANCE FREE SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71745-001
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)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71745-001-02	2 in 1 BOX	09/25/2017
1	NDC: 71745-001-01	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 NOT FINAL	part333E	09/25/2017

Labeler - GoodEarth Distribution Llc (079808558)

Registrant - Innocore Sales & Marketing Inc (201152597)