CROCODILECLOTH HAND SANITIZER- ethyl alcohol gel

CrocodileCloth Hand Sanitizer by

Drug Labeling and Warnings

CrocodileCloth Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Nuvik Usa, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

INDICATIONS & USAGE

Use to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Stop use and ask a doctor if irritation or redness develops.

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

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

Directions

Squeeze small amount in palm of hand and briskly rub hands together until dry.

Inactive Ingredients

Aloe Vera, Carbomer, Coconut Oil, Fragrance, Glycerin, Propylene Glycol, Purified Water, Tocopheryl Acetate, Triethanolamine.

Questions or Comments?

Call (855) 55-CLOTH; (1-855-552-5684), M-F

SPL UNCLASSIFIED SECTION

FIERCELY CLEAN

KILLS 99.99% OF GERMS.

REDUCES BACTERIA.

FRESH SCENT.

Manufactured for:

Nuvik USA Inc

Columbus, OH

(855) 55-CLOTH

www.crocodilecloth.com

Made in USA

Packaging

INGREDIENTS AND APPEARANCE

CROCODILECLOTH HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74602-250
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
COCONUT OIL (UNII: Q9L0O73W7L)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74602-250-12	370 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Nuvik Usa, Inc. (117472505)