Sanafitil Talco description, usages, side effects, indications, overdosage, supplying and lots more!

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Sanafitil Talco

ZURICH MEDICAL LABS, LLC

Sanafitil Talco


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredients Purpose
Undecylenic Acid 2% Antifungal
Zinc Undecylenate 20% Antifungal

Sanafitil Talco Uses

  • Cures most athlete's foot, jock itch & ringworm
  • Relieves itching, burning, cracking, and discomfort which accompany these conditions

Warning

  • For external use only.
  • Not for diaper rash
  • When using this product avoid contact with eyes and mucous membrane.
  • Do not use on children under 2 years of age except under the advice and supervision of a doctor.

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.

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 & 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

Other ingredients

talc

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label

SANAFITIL®

ANTIFUNGAL
POWDER

  • Treats most Athlete's foot, Jock itch & Ringworm

NET WEIGHT / PESO
NETO : 2 OZ (57 g)

Sanafitil Talco

Sanafitil Talco

UNDECYLENIC ACID and ZINC UNDECYLENATE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61357-152
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
UNDECYLENIC ACID 20 mg
ZINC UNDECYLENATE UNDECYLENIC ACID 200 mg

Inactive Ingredients

Ingredient Name Strength
talc

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 57 in 1 BOTTLE
2 NDC:61357-152-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 1966-08-24


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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