HAND SANITIZER 70 PERCENT- ethyl alcohol solution

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by AmmMm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70%

PURPOSE

ANTIBACTERIAL

FUNCTION:

70% ALCOHOL HAND SANITIZERS KILL MOST BACTERIA, AND FUNGI AND STOP SOME VIRUSES, KILL 99.9% OF THE BACTERIA ON HANDS 30 SECONDS AFTER APPLICATION AND 99.99% TO 99.999% IN ONE MINUTE.

Warnings

FOR EXTERNAL USE ONLY

KEEP AWAY FROM HEAT, FIRE OR FLAME.

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

STOP USE AND ASK A DOCTOR: IF IRRITATION OR REDNESS DEVELOPS OR IF CONDITION PERSISTS FOR MORE THAN 72 HOURS.

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.

Directions

• APPLY AMOUNT OF SANITIZER IN YOUR PALM TO THOROUGHLY COVER YOUR HANDS
• RUB HANDS TOGETHER BRISKLY UNTIL DRY
• NO RINSING REQUIRED
• FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION AND DON'T ALLOW THEM TO PUT THEIR HANDS IN THEIR MOUTH UNTIL THE PRODUCT EVAPORATES AND FEELS COMPLETELY DRY ON THE SKIN TO AVOID ACCIDENTAL INGESTION
• NOT RECOMMENDED FOR INFANTS

Inactive ingredients

AQUA, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, AMINOMETHYL PROPANOL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  70 PERCENT
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77397-101
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77397-101-11	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/06/2020

Labeler - Ammmm, Inc. (808060680)