Label: HC MAX ANTI-FUNGAL- tolnaftate aerosol, spray
- NDC Code(s): 55505-195-62
- Packager: Kramer Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 26, 2024
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Warnings
- WARNINGS
- WHEN USING
- STOP USE
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions ■ wash affected area and dry thoroughly ■ shake can well and spray a thin layer over affected area twice daily (morning and night) ■ 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 ■ use daily for 4 weeks ■ if condition persists, consult a doctor ■ to prevent athlete's foot, apply once or twice daily (morning and/or night) ■ This product is not effective on the scalp or nails.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL
Maximum Strength
HC MAX™
Tolnaftate Anti-Fungal Spray
FOR
ATHLETE'S
FOOT
Clinically Proven To
Cure AND
Prevent
Most Athlete's Foot
Cools
On Contact
Triple Action
Formula Relieves
✓ Itching
✓ Burning
✓ Cracking
NET WT 5.3 OZ (150 g)
KRAMER
LABORATORIES
Distributed by:
Kramer Laboratories, Inc.
Bridgewater, NJ 08807
1-800-824-4894
K0521 -
INGREDIENTS AND APPEARANCE
HC MAX ANTI-FUNGAL
tolnaftate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-195 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV) Tolnaftate 1.5 g in 150 g Inactive Ingredients Ingredient Name Strength Butylated Hydroxytoluene (UNII: 1P9D0Z171K) Isobutane (UNII: BXR49TP611) Ppg-12-Buteth-16 (UNII: 58CG7042J1) Alcohol (UNII: 3K9958V90M) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-195-62 150 g in 1 CAN; Type 0: Not a Combination Product 05/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 05/28/2020 Labeler - Kramer Laboratories (122720675)