HUSKY 515 Instant Hand Sanitizer

Dosage form: gel
Ingredients: alcohol 600mL in 1L
Labeler: Canberra Corporation
NDC Code: 63779-515

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.

Drug Facts

Active Ingredient:

Ethanol (60% v/v)

Purpose:

Anti-Microbial Hand Sanitizer

Uses
  • Helps reduce bacteria that potentially can cause disease
  • Helps prevent cross contamination by hand contact
  • Recommended for repeated use

Warnings
  • For external use only
  • Flammable, keep away from fire, heat, or flame

  • Keep out of reach of children.

Do not use near eyes
  • In case of eye contact flush with water for 15 minutes
  • If irritation persists stop use of product and get medical attention
  • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

Directions
  • Use no water or towels
  • Apply appropriate amount of product to palm of hand
  • Rub until hands are completely covered
  • Agitate lightly until dry
  • Let air dry for 15 seconds
  • Do not rinse or wipe with towel.

Other Information
  • Store in a cool dry place below 104° F.

Inactive Ingredients

Water, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

Principal Display Panel

Bottle Label

HUSKY®

515

INSTANT HAND

SANITIZER

(GEL-TYPE)

  • Enhanced with Moisturizers
  • Kills disease causing germs within seconds
  • Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
  • Assists with OSHA Bloodborne Pathogen Standard Compliance

For Hospital and Professional Use Only

See Drug Facts panel for additional information.

HUSKY 515   INSTANT HAND SANITIZER
ethanol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-515
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
alcohol (alcohol) alcohol600 mL  in 1 L
Inactive Ingredients
Ingredient NameStrength
water 
carbomer homopolymer type c 
aloe 
trolamine 
Packaging
#Item CodePackage Description
1NDC:63779-515-053.785 L in 1 BOTTLE
2NDC:63779-515-150.044 L in 1 BOTTLE
3NDC:63779-515-270.118 L in 1 BOTTLE
4NDC:63779-515-620.237 L in 1 BOTTLE
5NDC:63779-515-800.800 L in 1 BAG
6NDC:63779-515-880.237 L in 1 BOTTLE
7NDC:63779-515-890.490 L in 1 BOTTLE
8NDC:63779-515-201.100 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/28/1998
Labeler - Canberra Corporation (068080621)
Establishment
NameAddressID/FEIOperations
Canberra Corporation068080621MANUFACTURE

Revised: 08/2011
 
Canberra Corporation

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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