Label: HC MAX FOR JOCK ITCH- tolnaftate ointment
- NDC Code(s): 55505-194-26
- Packager: Kramer Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 29, 2023
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions ■ Clean the affected area with soap and warm water and dry thoroughly. ■ Apply a thin layer of HC Max™ Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor. ■ Supervise children in the use of this product. ■ For jock itch, use daily for 2 weeks. ■ If condition persists longer, consult a doctor. ■ This product is not effective on the scalp or nails.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
HC MAX™
Anti-Fungal Ointment
Ungüento Anti-Hongos
Tolnaftate 1%
FOR
JOCK ITCH
Clinically Proven to
CURE Most Jock Itch
Probado Clínicamente para Curar
La Mayoria de Casos de
Tiña Inguinal
plus
Aloe & Tea Tree Oil
for skin health
CLINICALLY PROVEN INGREDIENT
Relives
✓ Itching
✓ Burning
✓ Scaling
✓ Chafing
Alivia
✓ Picazón
✓ Ardor
✓ Descamación
✓ Agrietamientó
NET WT 1 OZ (28g)
Probado Clínicamente
para Curar
La Mayoria de
Casos de Tiña
Inguinal
más
Aloe y aceite de árbol de té
para la salud de la piel
HC MAX™
Ungüento anti-hongos
es infundido con 5 aceites
naturales que incluyen
árbol de té, eucalipto,
aloe, oliva y lavanda.
KRAMER
LABORATORIES
Distributed by:
Kramer Laboratories, Inc.
Bridgewater, NJ 08807
kramerlabs.com
funginail.com
1-800-824-4894
K0220
KRAMER
LABORATORIES
Kramer Laboratories, Inc. Bridgewater, NJ 08807 1-800-824-4894
Maximum Strength / Máxima Potencia
HC MAX™ FOR JOCK ITCH
Anti-Fungal Ointment / Ungüento Anti-Hongos
Tolnaftate 1%
NET CONTENT 1 OZ. (28 G)
K0220
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INGREDIENTS AND APPEARANCE
HC MAX FOR JOCK ITCH
tolnaftate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-194 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV) Tolnaftate 1 g in 100 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Carbomer Homopolymer Type A (Allyl Pentaerythritol Crosslinked) (UNII: F68VH75CJC) Dimethicone 350 (UNII: 2Y53S6ATLU) Eucalyptol (UNII: RV6J6604TK) Glyceryl Monostearate (UNII: 230OU9XXE4) Lavender Oil (UNII: ZBP1YXW0H8) Olive Oil (UNII: 6UYK2W1W1E) Phenoxyethanol (UNII: HIE492ZZ3T) Poloxamer 188 (UNII: LQA7B6G8JG) Water (UNII: 059QF0KO0R) Sodium Hydroxide (UNII: 55X04QC32I) Tea Tree Oil (UNII: VIF565UC2G) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-194-26 1 in 1 CARTON 06/01/2020 1 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 06/01/2020 Labeler - Kramer Laboratories (122720675)