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Name:Aftermath Hand Sanitizer
Manufacturer:Aftermath Inc.
Category:Over-the-counter (OTC) Marketed Drugs


Drug Facts

AFTERMATH HAND SANITIZER - ethanol gel 
Aftermath 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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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

Warning

  • 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

Aftermath Hand Sanitizer - label

Aftermath

Hand Sanitizer

800-366-9923

Specialists in crime scene and tragedy cleanup

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

For Hospital and Professional Use Only

See Drug Facts panel for additional information.

www.aftermath.com

Aftermath Hand Sanitizer - label

AFTERMATH HAND SANITIZER 
husky 515 gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:52188-515
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ethanol (ethanol) ethanol 600 mL  in 1000 mL
Inactive Ingredients
Ingredient Name Strength
water  
carbomer homopolymer type c  
aloe  
trolamine  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52188-515-88 237 mL in 1 BOTTLE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333 03/21/2010

Labeler - Aftermath Inc. (021860031)
Registrant - Aftermath Inc. (021860031)
Establishment
Name Address ID/FEI Operations
Canberra Corporation 068080621 MANUFACTURE

Revised: 04/2010 Aftermath Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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