Label: MICOTRIN AL- tolnaftate liquid
- NDC Code(s): 59088-477-03
- Packager: PureTek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated January 11, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
-
Uses
- for the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis).
- relieves itching, burning, cracking, scaling, and discomfort which accompany these conditions.
- for the prevention of most Athlete’s foot with daily use.
- eliminates fungus on fingers, toes, and around the nails.
- eliminates and helps stop the spread of fungal infections on cuticles around nail edges and under the nail tips where reachable with applicator brush.
- Warnings
-
Directions
- clean the affected area and dry thoroughly
- apply a thin layer of the product over affected area twice daily (morning and night) paying special attention to the edges of the nail, cuticles, and skin around the nails or as directed by a doctor
- 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
- for athlete's foot and ringworm, use daily for 4 weeks
- if condition persists longer, consult a doctor.
Use under the direction of a medical practitioner
- Other information
- How Supplied
- Inactive ingredients
- Micotrin AL™
-
INGREDIENTS AND APPEARANCE
MICOTRIN AL
tolnaftate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-477 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 0.3 g in 30 mL Inactive Ingredients Ingredient Name Strength ARGAN OIL (UNII: 4V59G5UW9X) BENZYL ALCOHOL (UNII: LKG8494WBH) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) DIMETHYL SULFOXIDE (UNII: YOW8V9698H) EUCALYPTUS OIL (UNII: 2R04ONI662) GLYCERIN (UNII: PDC6A3C0OX) LAURETH-4 (UNII: 6HQ855798J) LAVENDER OIL (UNII: ZBP1YXW0H8) TEA TREE OIL (UNII: VIF565UC2G) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) APPLE CIDER VINEGAR (UNII: 0UE22Q87VC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-477-03 30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 10/25/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 10/25/2021 Labeler - PureTek Corporation (785961046)