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Over-the-counter medicine

Butenafine Brand names: Lotrimin; first approved as Mentax

Butenafine (Lotrimin) is an over-the-counter medicine with an FDA approval on record since 1996. FDA's NDC Directory lists it from 13 generic labelers, and pharmacies paid $0.419 per gram (Butenafine HCl 1% cream) in the October 7, 2026 NADAC survey.

  • Generic listed
  • Over the counter

Check it at the source: the butenafine FDA label on DailyMed (effective December 5, 2025, Bayer Healthcare LLC.); the NDA 20524 record on Drugs@FDA; every butenafine label on DailyMed.

Highlights of the record

FDA label of December 5, 2025; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026; NADAC October 7, 2026

Used for

From the label: indications and usage

cures most jock itch relieves itching, burning, cracking, and scaling which accompany this condition

Forms and strengths

  • 1 g/100g
  • 10 mg/g

Cream.

On the market

Earliest approval on file
October 18, 1996 Mentax, Pharmobedient; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
1 first November 16, 2017; 1 with a marketed status in Drugs@FDA
Labelers listed (NDC)
14 of which 13 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
$0.419 per gram Butenafine HCl 1% cream
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
586 through July 30, 2026

What is butenafine used for?

From the label: indications and usage

cures most jock itch relieves itching, burning, cracking, and scaling which accompany this condition

FDA pharmacologic class: Benzylamine Antifungal.

Source: FDA drug label (Lotrimin Ultra Jock Itch), Bayer Healthcare LLC., effective December 5, 2025 (SPL set 9dfa08fb-0913-4326-b1eb-1425df6a2c82), via openFDA; the full label on DailyMed

Is there a generic for butenafine (Lotrimin)?

The FDA approved the first generic butenafine on November 16, 2017. 1 generic application is approved; 1 of it carries a current (not discontinued) marketing status in Drugs@FDA; that status is not evidence that the generic is on sale.

FDA's NDC Directory lists butenafine from 13 labelers under a generic (ANDA) application and from 1 brand labeler. A listing means the company has registered the product for sale; it does not show that every pharmacy stocks it.

  • 1996 earliest approval on file
  • 2017 first generic approved

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do pharmacies pay for butenafine (Lotrimin)?

In CMS's NADAC survey of October 7, 2026, pharmacies paid $0.419 per gram (Butenafine HCl 1% cream), up 28% from $0.328 on October 8, 2025. The chart's scale runs from the lowest to the highest price shown, not from zero. NADAC is what retail pharmacies paid their wholesalers, per unit, in CMS's monthly survey; what a patient pays depends on insurance and the pharmacy.

  • Butenafine HCl 1% cream (generic)
$0.421
$0.306
April 2024October 2026
NADAC per unit, October 7, 2026
Strength and formBrand or genericPharmacy cost30 tablets, or one pen or vial12-month change
Butenafine HCl 1% creamGeneric$0.419 per gramn/a+28%

Source: CMS National Average Drug Acquisition Cost (NADAC) survey, October 7, 2026: what retail pharmacies paid per unit; not a counter price

What do FAERS reports show for butenafine?

The FDA Adverse Event Reporting System holds 586 reports that list butenafine among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 7 are coded as a death and 24 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

Reports received each year

The most reported reactions

  • Drug Ineffective (a use or a product term, not a reaction)185
  • Off Label Use (a use or a product term, not a reaction)59
  • Product Use Issue (a use or a product term, not a reaction)44
  • Product Use In Unapproved Indication (a use or a product term, not a reaction)34
  • Pruritus33
  • Condition Aggravated (a use or a product term, not a reaction)29
  • Rash23
  • Drug Ineffective For Unapproved Indication (a use or a product term, not a reaction)20

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Butenafine side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other