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Sanafitil

Dosage form
OINTMENT
Labeler
ZURICH MEDICAL LABS, LLC
Label updated
2014-03-21
Retrieved
2026-09-07
Active ingredients
Undecylenic Acid
View original label and images on DailyMed ↗
Label information

Drug Facts

Active Ingredients

Undecylenic Acid 10%

Purpose

Antifungal

Uses
  • For the treatment of most athlete's foot, jock itch & ringworm
  • Relieves itching, burning, cracking, scaling and discomfort which accompany these conditions.
Warning
  • For external use only.

Label information

  • When using this product avoid contact with eyes and mucous membrane.

Label information

  • Do not use on children under 2 years of age except under the advice and supervision of a doctor.
  • Not for diaper rash

Label information

Stop use and ask a doctor if:

  • Irritation occurs
  • There is no improvement within 4 weeks of treatment for athlete's foot and ringworm and 2 weeks of treatment for jock itch discontinue use and consult a doctor.

Label information

KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion seek professional assistance or contact a poison control center right away.

Directions
  • Clean affected area and dry thoroughly.
  • Apply a thin layer over affected area twice daily (morning and night) or as directed by a doctor.
  • For athlete's foot pay special attention to the space between the toes. Wear well fitting, ventilated shoes and change shoes & socks at least once a day.
  • For athlete's foot and ringworm, use daily for 4 weeks
  • For jock itch use daily for 2 weeks.
  • Supervise Children in use of this product.
  • Product not effective in the scalp or nails.
Other Information

Store at 59° - 86° F (15°- 30°C)

Other ingredients

petrolatum white, benzocaine, paraffin wax, salicylic acid, benzoic acid, boric acid, methyl salicylate, methyl paraben, propyl paraben, menthol crystals

PRINCIPAL DISPLAY PANEL - 28.35 g Tube Carton

SANAFITIL®
(Undecylenic Acid 10%)

ANTIFUNGAL

OINTMENT

1 OZ. (28.35g)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 62ef352c-0cc4-400a-94e2-24777638589a · Version 1
NDC: 61357-149