INOCULEX HAND SANITIZER- ethyl alcohol liquid

Inoculex Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 70%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use as hand sanitizer to help reduce bacteria on the skin

WARNINGS

Warnings

Flammable, keep away from fire or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

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

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

DOSAGE & ADMINISTRATION

Directions apply palmful to hands rub hands together vigorously until dry supervise children in the use of this product.

STORAGE AND HANDLING

Other Information store below 110°F (43°C)  may discolor certain fabrics or surfaces.

INACTIVE INGREDIENT

Inactive ingredients: Fragrance, Glycerol, Hydrogen Peroxide, *Hydroxypropyl Cellulose, *Hydroxypropyl Methycellulose, Water

*May or may not include

SPL UNCLASSIFIED SECTION

www.inoculex.com

Distributed by: Inoculex, LLC

16 S Pennsylvania Ave.,

Oklahoma City, OK 73107

Made in the USA

Packaging

INGREDIENTS AND APPEARANCE

INOCULEX HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77017-015
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77017-015-02	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020
2	NDC: 77017-015-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020
3	NDC: 77017-015-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020
4	NDC: 77017-015-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020
5	NDC: 77017-015-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020
6	NDC: 77017-015-28	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/13/2020

Labeler - Private Label Supplements (081035641)