INITIAL TREATONIC FUNGAL NAIL RENEWAL PATCHES- tolnaftate 1% patch

Initial Treatonic FUNGAL NAIL RENEWAL PATCHES by

Drug Labeling and Warnings

Initial Treatonic FUNGAL NAIL RENEWAL PATCHES by is a Otc medication manufactured, distributed, or labeled by 100 KARMA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate 1%

PURPOSE

Antifungal

DOSAGE & ADMINISTRATION

• Helps inhibit the growth of fungus.
• Improves the appearance of nails affected by fungus,including discoloration, thickening, splitting, crumbing, and brittleness.

WARNINGS

For external use only

• on children under 2years of age unless directed lby a doctor
• on dliaper rash

Avoid contact with eyes. do not exceed the recommended daily dosage unless directed by a doctor.

• iritation occurs
• there is no improvement within 4 weeks.

ask a health professional before use.

In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.

INDICATIONS & USAGE

• Clean & prepare the affected nail,
• Applythe antifungal solution to the affected nail.
• Apply the fungus nail patch, Fimly secure the patch to the sides of the toes or fingers,folding the remaining achesive partto fully cover the toes/fingertips.
• Leave the patch on for 6-8 hours.Frequency. Use the patches consistently before bed.
• Maintain good foothygiene.

OTHER SAFETY INFORMATION

store at 20-25°C(68-77°F)

INACTIVE INGREDIENT

Water, Glycerin, Sodium Carboxymethyl Cellulose,Butylene Glycol, Urea

QUESTIONS

Email: service@treatonic.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

INITIAL TREATONIC FUNGAL NAIL RENEWAL PATCHES 
tolnaftate 1% patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85569-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 mg  in 100

Inactive Ingredients
Ingredient Name	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85569-013-01	32 in 1 PATCH; Type 0: Not a Combination Product	02/18/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	02/18/2026

Labeler - 100 KARMA INC (120186232)