Label: FUNGI NAIL EVERYDAY ANTIFUNGAL POWDER- tolnaftate spray
- NDC Code(s): 55505-234-81
- Packager: Kramer Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 24, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions
■ To prevent athlete's foot, wash and dry feet thoroughly
■ Shake can well and spray 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.
■ Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
■ In case of clogging, clean nozzle with pin.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
NEW MAXIMUM STRENGTH
FUNGI
NAIL®
TOLNAFTATE ANTI-FUNGAL
EVERYDAY
TOE & FOOT ANTI-FUNGAL
POWDER SPRAY
STOPS
FOOT FUNGUS
BEFORE IT
CAN SPREAD
Use Daily To Prevent
Most Athlete's Foot
▪ Absorbs Wetness
To Fight Odor
▪ Talc-free
NET WT 4.6 OZ (130 g)
Not for nail or scalp fungus.
For more information about
Fungi-Nail® and money back
guarantee, visit us at funginail.com
Dist. by: Kramer Laboratories, Inc.
Bridgewater, NJ 08807
1-800-824-4894
K0524

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INGREDIENTS AND APPEARANCE
FUNGI NAIL EVERYDAY ANTIFUNGAL POWDER
tolnaftate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-234 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 Butylated Hydroxytoluene (UNII: 1P9D0Z171K) Isobutane (UNII: BXR49TP611) Kaolin (UNII: 24H4NWX5CO) Ppg-12-Buteth-16 (UNII: 58CG7042J1) Alcohol (UNII: 3K9958V90M) Zea Mays Whole (UNII: 1G5HNE09V8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-234-81 130 g in 1 CAN; Type 0: Not a Combination Product 01/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 01/01/2025 Labeler - Kramer Laboratories (122720675)
