HAND SANITIZER 70 PERCENT- ethyl alcohol solution 
AmmMm, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ALCOHOL HAND SANITIZER GEL - 70% Ethyl Alcohol

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. 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

01b LBL_Hand sanitizer_1 gal

HAND SANITIZER  70 PERCENT
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77397-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77397-102-113785 mL in 1 BOTTLE; Type 0: Not a Combination Product08/21/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/21/2020
Labeler - AmmMm, Inc. (808060680)

Revised: 8/2020
 
AmmMm, Inc.