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Handi-Sani by Chromate Industrial Corporation

Dosage form: liquid
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: Chromate Industrial Corporation
NDC Code: 76063-738

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.

Handi-Sani 6738 Drug Facts and Label

Drug Facts Box OTC-Active Ingredient Section

Ethyl Alcohol 62%

Drug Facts Box OTC-Purpose Section

Antiseptic

Drug Facts Box OTC-Indications and Usage Section

for hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

Flammable, keep away from fire and flames

For external use only

Drug Facts Box OTC-When Using Section

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box OTC-Stop Use Section

irritation and redness develop

Drug Facts Box OTC-Keep Out of Reach of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box OTC-Dosage & Administration Section

Wet hands thoroughly with product and allow to dry without wiping

Drug Facts Box OTC-Inactive Ingredient Section

water, propylene glycol, fragrance, acid blue 25

Handi-Sani 6738 4 oz

6738Z8P90046.jpg   Handi-Sani  4oz 

HANDI-SANI  
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76063-738
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:76063-738-143785 mL in 1 BOTTLE, PLASTIC
2NDC:76063-738-15946 mL in 1 BOTTLE, PLASTIC
3NDC:76063-738-16236 mL in 1 BOTTLE, PLASTIC
4NDC:76063-738-17532 mL in 1 BOTTLE, PLASTIC
5NDC:76063-738-1850 mL in 1 BOTTLE, PLASTIC
6NDC:76063-738-24118 mL in 1 BOTTLE, PLASTIC
7NDC:76063-738-55208200 mL in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/01/2011
Labeler - Chromate Industrial Corporation (061955621)
Registrant - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIOperations
ABC Compounding Co., Inc.003284353manufacture

Revised: 04/2011
 
Chromate Industrial Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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