Label: AFTERMATH HAND SANITIZER- husky 515 gel
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Contains inactivated NDC Code(s)
NDC Code(s): 52188-515-88 - Packager: Aftermath Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 Label Information
Updated April 2, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient:
- Purpose:
- Uses
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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
- Other Information
- Inactive Ingredients
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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
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INGREDIENTS AND APPEARANCE
AFTERMATH HAND SANITIZER
husky 515 gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52188-515 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ethanol (UNII: 3K9958V90M) (ethanol - UNII:3K9958V90M) ethanol 600 mL in 1000 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) carbomer homopolymer type c (UNII: 4Q93RCW27E) aloe (UNII: V5VD430YW9) trolamine (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52188-515-88 237 mL in 1 BOTTLE 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 Business Operations Canberra Corporation 068080621 MANUFACTURE