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Bengama Antifungal

Dosage form: solution
Ingredients: TOLNAFTATE 1mg in 100mL
Labeler: Genuine Drugs
NDC Code: 69666-831

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 (in each gram)

Tolnaftate 1%

Purpose

Antifungal

Uses
  • clinically proven to cure most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • helps prevnet most athlete's foot from recurring when used daily
  • effectively soothes and relieves symptoms of athlete's foot, including itching, burning and cracking

Warnings

For external use only

When using this product

avoid contact with the eyes

Stop use and ask a doctor if
  • irritation occurs
  • there is no improvement within 4 weeks

Do not use

on children under 2 years of age except under the advice and supervision of a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • shake well before using
  • apply generously to affected areas and massage gently until liquid is absorbed into the skin
  • for adults and children over 12, rub well on the afffected area. repeat 3-4 times daily
  • for children 12 years of age or younger, consult a doctor before use

Inactive ingredients

dehydrated ethyl alcohol, butylated hydroxytoluene, polyethylene glycol

Other information
  • store at controlled room temperature

Package label

Bengama antifungal

BENGAMA ANTIFUNGAL 
tolnaftate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69666-831
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (TOLNAFTATE) TOLNAFTATE1 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE 
POLYETHYLENE GLYCOLS 
Packaging
#Item CodePackage Description
1NDC:69666-831-041 BOTTLE in 1 BOX
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C04/20/2015
Labeler - Genuine Drugs (079610378)

Revised: 11/2017
 
Genuine Drugs

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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