PHARMLITALIA ANTIFUNGAL MEDICATED BODY- tolnaftate cloth

Pharmlitalia Antifungal Medicated Body by

Drug Labeling and Warnings

Pharmlitalia Antifungal Medicated Body by is a Otc medication manufactured, distributed, or labeled by Foshan Sugar Max Cosmetics CO.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                                           

Tolnaftate 1%

Purpose

Antifungal

Uses

Meticulously formulated to serve as a potent disinfectant solution.
By significantly reducing bacterial presence, these wipes foster superior hygiene practices, offering an added layer of protection specifically designed for athletes.

Warnings

For external use only

Do not use:
On scalp
In or near the mouth or eyes
For vaginal yeast infections

When using this product:
Do not get into eyes. If eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if: irritation occurs or worsens.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

Open lid and pull out one wipe. Gently cleanse the desired area. Discard wipe after use (do not flush).
Close lid tightly to keep wipes moist.

Other Information

• Do not use if seal on bottle is broken or is not visible.
• Store at controlled room temperature 20–25°C (68–77°F).

Other Information

Tea Tree Oil, Distilled Water , Eucalyptus Oil, Coco Glucoside

Product label

INGREDIENTS AND APPEARANCE

PHARMLITALIA ANTIFUNGAL MEDICATED BODY 
tolnaftate cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84938-010
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 mL

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
WATER (UNII: 059QF0KO0R)
EUCALYPTUS OIL (UNII: 2R04ONI662)
COCO-GLUCOSIDE (UNII: ICS790225B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84938-010-01	40 in 1 BOTTLE	10/30/2025
1		3.5 mL in 1 PATCH; 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	10/30/2025

Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)