INOCULEX HAND SANITIZER- ethyl alcohol gel

Inoculex Hand Sanitizer by

Drug Labeling and Warnings

Inoculex Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Private Label Supplements, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use(s)

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

On children less than 2 months of age

On open skin wound

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation occurs. these may be signs of a serious condition.

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

Directions

Place enough product on hands to cover all surfaces. Rub hand together until dry.

Supervise children under 6 years of age when using the product to avoid swallowing.

Other information

Store between 15-30C (59-86F)

Avoid Freezing and excessive heat above 40C (104F) 

Inactive ingredients

carbomer, glycerin, water

SPL UNCLASSIFIED SECTION

With 70% Ethyl Alcohol

FRAGRANCE FREE

NEVER TESTED ON ANIMALS

VEGAN LIFESTYLE FRIENDLY

SULFATE-FREE

PARABEN-FREE

HOSPITAL GRADE FORMULA

Apply   Massage   Conquer

Distributed by: Inoculex, LLC

16 S Pennsylvania Ave.,

Oklahoma City, OK 73107

www.inoculex.com

Made in the USA

Packaging

INGREDIENTS AND APPEARANCE

INOCULEX HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77017-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77017-014-28	3.78 L in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/15/2021

Labeler - Private Label Supplements, Llc (081035641)