Active Ingredient (In Each Gram)
Tolnaftate 1%
Bengama Antifungal
FDA Label NDC 69666-831
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine Drugs for the product Bengama Antifungal (NDC 69666-831). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each gram), purpose, uses, warnings, when using this product, stop use and ask a doctor if, do not use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
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