NINETEEN CERTIFIED HAND SANITIZER- alcohol liquid

Nineteen Certified Hand Sanitizer by

Drug Labeling and Warnings

Nineteen Certified Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Lopez-Scripa Industries LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 80%

PURPOSE

Antiseptic

INACTIVE INGREDIENTS

17-18% Sterilized Water, 1.5 % Glycerin 0.2% Hydrogen Peroxide 34%, Less than 0.01% Bittering Agent

USES

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

DIRECTIONS

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Do not use on children less than 2 months of age. Do not use on open wounds.

WARNINGS

FOR EXTERNAL USE ONLY - HANDS

FLAMMABLE - KEEP AWAY FROM HEAT AND FLAME

WHEN USING THIS PRODUCT

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

STOP USE AND ASK A DOCTOR

if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF THE REACH OF CHILDREN

If swallowed, seek medical help or contact a Poison Control Center right away.

OTHER INFORMATION

Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C). May discolor some fabrics. Harmful to wood finishes and plastics.

Package Labeling:

INGREDIENTS AND APPEARANCE

NINETEEN CERTIFIED HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79526-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79526-000-01	3785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/08/2020

Labeler - Lopez-Scripa Industries LLC (036115985)