KLEANN GO HAND SANITIZER JOJOBA AND VIT E- ethyl alcohol gel

KleanN Go Hand Sanitizer by

Drug Labeling and Warnings

KleanN Go Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sanihealth Labs Inc., SaniHealth Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 70%v/v.

Purpose: Antiseptic

Purpose

Antiseptic

Uses

• For topical use. Use as part of your daily cleansing routine when soap and water are not available, or to supplement hand-washing. For occasional and personal domestic use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Safety Instructions

Flammable, Keep away from fire and flame

Ask Doctor

Stop Use and Ask a doctor if irritation or redness develops

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact Poison Control right away

Directions

• For adults on children over 2 years: supervise children when using this product. Apply liberally and rub thoroughly into hand for 30 seconds. Allow to dry

Other Information

For Questions

Call- 1-833-826-2586

Inactive Ingredients

water, hydrolyzed jojoba esters, glycerin, carbopol, fragrance, aminomethyl propanol, denatonium benozate, tocopherol acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KLEANN GO HAND SANITIZER  JOJOBA AND VIT E
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79861-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79861-002-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/10/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/10/2021

Labeler - Sanihealth Labs Inc. (204172811)

Establishment
Name	Address	ID/FEI	Business Operations
SaniHealth Labs Inc		204172811	manufacture(79861-002)