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Joch Itch Antifungal Quinsana

Dosage form: powder
Ingredients: Tolnaftate 1g in 100g
Labeler: Product Quest Mfg
NDC Code: 64048-2479

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                                                   Purpose
Tolnaftate, 1% ....................................................... Antifungal

• Cures most athlete’s foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)
• Effectively relieves • Itching • Cracking • Burning

For external use only
Ask a doctor before use • On children under 2 years of age When using this product • Avoid contact with eyes
Stop use and ask a doctor if • Irritation occurs • There is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

• Wash affected area and dry thoroughly.
• Apply a thin layer of the product over time indicated.
• Supervise children in the use of this product.
For athlete’s foot and ringworm: Use twice daily (morning and night) for 4 weeks or as directed by physician. Pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
For jock itch: Use daily for 2 weeks. • Clean the affected area and dry thoroughly. • This product is not effective on the scalp or nails.

Inactive ingredient: Talc, Cornstarch

tolnaftate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64048-2479
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Tolnaftate (TOLNAFTATE) Tolnaftate1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:64048-2479-385 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C06/15/2015
Labeler - Product Quest Mfg (927768135)
Ei LLC105803274manufacture(64048-2479)

Revised: 11/2017
Product Quest Mfg

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.