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 99.9% of the bacteria on hands with 2.5 ml of solution for 15 seconds after application.

Warnings

FOR EXTERNAL USE ONLY - HANDS

FLAMMABLE: 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 AND AVOID SWALLOW.

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
• NOT RECOMMENDED FOR INFANTS

Inactive ingredients

WATER, GLYCERIN, CARBOMER, AMINOMETHYL PROPANOL

OTHER INFORMATION:

• DO NOT STORE ABOVE 105 (DEGREES FAHRENHEIT)
• MAY CAUSE DISCOLORATION TO CERTAIN FABRICS AND SURFACES
• HARMFUL TO WOOD FINISHES AND PLASTICS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER   70 PERCENT
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77397-102
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77397-102-11	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
2	NDC: 77397-102-15	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
3	NDC: 77397-102-10	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
4	NDC: 77397-102-12	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
5	NDC: 77397-102-13	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
6	NDC: 77397-102-14	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/21/2020

Labeler - AmmMm, Inc. (808060680)