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Strawberry Scented Hand Sanitizer Crown

Dosage form: gel
Ingredients: BENZALKONIUM CHLORIDE 1g in 59g
Labeler: Townley, Inc.
NDC Code: 58737-145

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.

Disney Princess

Strawberry Scentend 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).

STRAWBERRY SCENTED HAND SANITIZER  CROWN
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58737-145
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
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:58737-145-0159 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/02/2016
Labeler - Townley, Inc. (016956158)
Establishment
NameAddressID/FEIOperations
Townley, Inc.016956158manufacture(58737-145)

Revised: 06/2016
 
Townley, Inc.

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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