Label: TOLNAFTATE- tolnaftate powder spray aerosol, spray
- NDC Code(s): 30142-841-01
- Packager: Kroger Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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
-
Warnings
For external use only.
Flammable:
Do not use while smoking or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
-
Directions
- wash affected area and dry thoroughly
- shake can well and spray a thin layer over affected area twice daily (morning and night) or as directed by a doctor
- supervise children in the use of this product
- to prevent athlete's foot, apply once or twice daily (morning and/or night)
- 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
- use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch
- if conditions persist, consult a doctor
- this product is not effective on the scalp or nails
- if nozzle clogs, clean with a pin
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
TOLNAFTATE
tolnaftate powder spray aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-841 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1.3 g in 130 g Inactive Ingredients Ingredient Name Strength ISOBUTANE (UNII: BXR49TP611) KAOLIN (UNII: 24H4NWX5CO) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PPG-12-BUTETH-16 (UNII: 58CG7042J1) ALCOHOL (UNII: 3K9958V90M) ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-841-01 130 g in 1 CAN; Type 0: Not a Combination Product 03/11/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 03/11/2022 Labeler - Kroger Co. (006999528)