Drug Labeling and Warnings

Drug Details

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KEEP IT CLEAN PURE CLEAN- alcohol solution 
G Mason Group LLC

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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ACTIVE INGREDIENT

ETHYL ALCOHOL 69%

PURPOSE

ANTISEPTIC

USES

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE RECOMMENDED FOR REPEATED USE.

WARNINGS

For external use only: hands

Flammable. Keep away from fire or flame.

When using this product

  • Keep out of eyes. In case of contact with eyes flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not ingest or inhale.

Stop use and ask a doctor if

  • irritation and redness develop
  • 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

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING.

  • FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION.
  • NOT RECOMMENDED FOR INFANTS.

OTHER INFORMATION

DO NOT STORE ABOVE 105 DEGREES F

  • MAY DISCOLOR SOME FABRICS
  • HARMFUL TO WOOD FINISHES AND PLASTICS

INACTIVE INGREDIENTS

WATER (AQUA), ALOE BARBADENSIS (ALOE VERA) LEAF JUICE, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, PROPANDIOL, AMINOMETHYL PROPANOL, TOCOPHERYL ACETATE

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KEEP IT CLEAN  PURE CLEAN
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73389-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL69 mL  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PROPANEDIOL (UNII: 5965N8W85T)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73389-103-11236 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/17/2019
Labeler - G Mason Group LLC (078797167)

Revised: 3/2020
 
G Mason Group LLC


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