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Hi Vetic by Sato Pharmaceutical Co., Ltd.

Medically reviewed by Last updated on Aug 22, 2019.

Dosage form: ointment
Ingredients: tolnaftate 1g in 100g
Labeler: Sato Pharmaceutical Co., Ltd.
NDC Code: 49873-056

Further information

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


Active ingredient    Tolnaftate 1%

Purpose    Antifungal

Uses ■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

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

■for the treatment 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

Inactive ingredients  Carboxymethylcellulose sodium, diethyl sebacate, fragrance, glyceryl monostearate, lauromacrogol 400, light mineral oil, polyoxyethylene cetylether, potassium stearate, propylene glycol, simethicone, sodium lauryl sulfate, stearyl alcohol, urea, water, white wax, zinc oxide.

tolnaftate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-056
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
tolnaftate (tolnaftate) tolnaftate1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
diethyl sebacate 
potassium stearate 
sodium lauryl sulfate 
glyceryl monostearate 
zinc oxide 
white wax 
stearyl alcohol 
light mineral oil 
propylene glycol 
#Item CodePackage Description
1NDC:49873-056-011 TUBE in 1 CARTON
115 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/25/1996
Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-056), label(49873-056), pack(49873-056)

Sato Pharmaceutical Co., Ltd.

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