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Hi Vetic by Sato Pharmaceutical Co., Ltd.

Dosage form: solution
Ingredients: tolnaftate 1g in 100mL
Labeler: Sato Pharmaceutical Co., Ltd.
NDC Code: 49873-050

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.


Purpose    Antifungal

■ for effective treatment of most athlete’s foot, jock itch, and ringworm ■prevents the recurrence of most athlete’s foot with daily use

For external use only
Extremely flammable. Keep away from fire or flame

Do not use
■on children under 2 years of age unless directed by a doctor

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 for athlete’s foot and ringworm, and within 2 weeks for jock itch

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

■for the tratment of athlete’s foot, jock itch, and ringworm
■cleanse the affected area with soap and water and dry throughly
■apply a thin layer of the product over affected area twice daily (morning and night), or as directed by a doctor
■to prevent athlete’s foot
■cleanse the feet with soap and water and dry throughly
■apply a thin layer of the product to the feet once or twice daily (morning and/or 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
■change shoes and socks at least once daily
■for athlete’s foot and ringworm, use daily for 4 weeks.
■for jock itch, use daily for 2 weeks.
■if condition persists longer, consult a doctor
■this product is not effective on the scalp or nails

Other information   
■keep tightly closed
■cap bottle tightly and store at room temperature away from heat

Inactive ingredients  acetone, citric acid, diethyl sebacate, fragrance, isopropyl alcohol, lauromacrogol 400, propyl gallate, water

Active ingredient
Tolnaftate 1%



tolnaftate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-050
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
tolnaftate (tolnaftate) tolnaftate1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
citric acid monohydrate 
diethyl sebacate 
isopropyl alcohol 
propyl gallate 
#Item CodePackage Description
1NDC:49873-050-021 BOTTLE (BOTTLE) in 1 CARTON
120 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C08/14/1990
Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
Sato Pharmaceutical Co., Ltd.715699133manufacture, label, pack

Revised: 01/2012
Sato Pharmaceutical Co., Ltd.

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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.