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MickMinn Forever 6 pack Hand Sanitizer

Medically reviewed on August 27, 2018

Dosage form: gel
Ingredients: BENZALKONIUM CHLORIDE 1g in 59g
Labeler: Townley, Inc.
NDC Code: 58737-176

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.

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose: Antibacterial

Use

To decrease bacteria on the skin that could cause disease.

Keep out of reach of children.

Hand Sanitizer

2 FL OZ (59mL)

Warnings

  • for external use only-hands.
  • keep out of eyes. avoid contact with broken skin.
  • stop use and ask a Doctor if irritation or redness develops.
  • do not inhale or ingest. if swallowed, get medical help or contact a poison control center right away.

Directions

  • Rub a dime sized drop into hands.
  • For children under 6 use under adult supervision.

Inactive Ingredients

water (aqua/eau), glycerin, coceth-7, PPG-1-PEG-9 lauryl glycol ether, carbomer, triethanolamine, PEG-40 hydrogenated castor oil, fragrance (parfum).

May Contain

Red 40 (CI 16035), Red 33 (CI 17200), Blue 1 (CI 42090), Yellow 5 (CI 19140).

MICKMINN FOREVER 6 PACK HAND SANITIZER 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58737-176
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 g  in 59 g
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE 
WATER 
GLYCERIN 
COCETH-7 CARBOXYLIC ACID 
PPG-1 TRIDECETH-6 
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) 
TROLAMINE 
PEG-40 CASTOR OIL 
PPG-1-PEG-9 LAURYL GLYCOL ETHER 
METHOXY PEG-40 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY, GRAPE, COTTON CANDY, LEMON, BUBBLE GUM, WATERMELONImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:58737-176-0159 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/25/2016
Labeler - Townley, Inc. (016956158)
Establishment
NameAddressID/FEIOperations
Townley, Inc.016956158manufacture(58737-176)

 
Townley, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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