HAND SANITIZER HOSPITAL AND INDUSTRIAL STRENGTH- ethyl alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by DIVERSIFIED MANUFACTURING CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 62%

PURPOSE

ANTIMICROBIAL

USES

HAND SANITIZER TO DECREASE BACTERIA ON THE SKIN THAT CAUSES DISEASE. RECOMMENDED FOR REPEATED USE.

WARNINGS

FOR EXTERNAL USE ONLY-HANDS.

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IN CASE OF CONTACT, FLUSH EYES THOROUGHLY WITH WATER.

DO NOT INHALE OR INGEST. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

WET HANDS THOROUGHLY WITH THE PRODUCT AND ALLOW IT TO DRY WITHOUT WIPING. CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

NOT RECOMMENDED FOR INFANTS.

OTHER INFORMATION

DO NOT STORE ABOVE 104°F (40°C).

MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

INACTIVE INGREDIENTS

PURIFIED WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, ALOE VERA GEL, ALOE VERA OIL, TOCOPHERYL ACETATE, FRAGRANCE.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  HOSPITAL AND INDUSTRIAL STRENGTH
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62172-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62172-115-13	89 mL in 1 TUBE; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/21/2020

Labeler - DIVERSIFIED MANUFACTURING CORP (185073996)