SANITIZETEK- isopropyl alcohol liquid

Sanitizetek by

Drug Labeling and Warnings

Sanitizetek by is a Otc medication manufactured, distributed, or labeled by Sanitizetek, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient
Isopropyl Alcohol, 75%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Uses
♦ Hand sanitizer to help reduce bacteria on the skin that could cause disease
♦ Recommended for repeated use

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 rash appears and persists

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

♦ Place enough product in your palm to thoroughly cover hands.
♦ Rub hands together briskly until dry.
♦ Children under 6 years of age should be supervised when using this product.

OTHER SAFETY INFORMATION

Other information: ♦ Do not store above 110° F (43° C)
♦ May discolor certain fabrics or surfaces

INACTIVE INGREDIENT

Inactive Ingredients:
Glycerin, Hydrogen Peroxide, Purified Water USP

Package Label

SanitizeTek

The Front Line in Sanitizer and Disinfectant Innovation

Hand Sanitizer

75% Isopropyl Alcohol Antiseptic

Spray with Hydrogen Peroxide

Meets FDA & WHO Guidelines.

Cover hands and allow to dry completely

2 fl oz (59 mL)

www.sanitizeTek.com          (888) 7000-TEK

Packed by: SanitizeTek, LLC
109C Shooting Club Rd., Boerne, TX 78006

2 OZ

16.9 OZ

1 GAL

55 GAL

330 GAL

res

INGREDIENTS AND APPEARANCE

SANITIZETEK 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81737-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.750 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81737-002-01	0.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/22/2021
2	NDC: 81737-002-02	0.500 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/22/2021
3	NDC: 81737-002-04	3.7 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/22/2021
4	NDC: 81737-002-05	208 L in 1 DRUM; Type 0: Not a Combination Product	03/22/2021
5	NDC: 81737-002-06	6705 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	03/22/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/22/2021

Labeler - Sanitizetek, LLC (117613908)

Registrant - Sanitizetek, LLC (117613908)

Establishment
Name	Address	ID/FEI	Business Operations
Sanitizetek, LLC		117613908	repack(81737-002) , label(81737-002)