Tolnaftate by Premier Brands of America Inc.
Medically reviewed on Jan 1, 2018
Dosage form: aerosol, powder
Ingredients: TOLNAFTATE 1.3g in 130g
Labeler: Premier Brands of America Inc.
NDC Code: 56104-527
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.
- cures most jock itch (tinea cruris)
- relieves itching, burning and chafing associated with jock itch
For external use only.
Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF.
- do not get into eyes or mouth
- use only as directed
Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.
- irritation occurs
- no improvement within 2 weeks for jock itch
If swallowed, get medical help or contact a Poison Control Center right away. Do not use on children under 2 years of age. Do not use for diaper rash.
- wash affected area and dry thoroughly
- shake can well and spray a thin layer over affected area twice daily (morning and night)
- supervise children in the use of this product
- use daily for 2 weeks; if conditions persist, consult a doctor
- in case of clogging, clear nozzle under running water
store between 20º and 30ºC (68ºF and 86º)
BHT, isobutane (propellent), PPG-12-buteth-16, SD alcohol 40-B (14%w/w), talc
medicated jock itch powder spray aerosol, powder
|Labeler - Premier Brands of America Inc. (080051232)|
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