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Tinactin Super Absorbent

Medically reviewed on August 14, 2017

Dosage form: powder
Ingredients: TOLNAFTATE 10mg in 1g
Labeler: Bayer HealthCare LLC.
NDC Code: 11523-4362

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.

Tinactin Super Absorbent Powder

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses
  • proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • helps prevent most athlete's foot with daily use
  • for effective relief of itching, burning and cracking

Warnings

For external use only

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
  • wash affected area and dry thoroughly
  • apply a thin layer over affected area twice daily (morning and night)
  • supervise children in the use of this product
  • for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily
  • use daily for 4 weeks; if condition persists longer, ask a doctor
  • to prevent athlete's foot, apply once or twice daily (morning and/or night)
  • this product is not effective on the scalp or nails

store between 20° to 25°C (68° to 77°F)

benzethonium chloride, corn starch, kaolin, sodium bicarbonate

Questions? 1-866-360-3266

TINACTIN  SUPER ABSORBENT
tolnaftate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4362
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (TOLNAFTATE) TOLNAFTATE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE 
SODIUM BICARBONATE 
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) 
KAOLIN 
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:11523-4362-1108 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C09/23/1993
Labeler - Bayer HealthCare LLC. (112117283)

 
Bayer HealthCare LLC.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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