Kiss Fungi-gone
FDA Label NDC 42432-101

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kiss Products, Inc. for the product Kiss Fungi-gone (NDC 42432-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, do not use and ask doctor if:, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Uses

→ Warnings

→ Do Not Use

→ Do Not Use And Ask Doctor If:

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Image Of Labels And Cartons

Active Ingredient

Tolnaftate 1%

Purpose

Anti-fungal

Uses

For the cure of:

athlete's foot (tinea pedis)
jock itch (tinea cruris)
ringworm (tinea corporis)

For the relief of:

itching
cracking
burning
scaling
discomfort associated with the above condition

Warnings

For external use only. Avoid contact with eyes.

Do Not Use

for bacterial infections
for diaper rash
on children under 2 years of age unless directed by a doctor

Do Not Use And Ask Doctor If:

irritation occurs
there is no improvement within 4 weeks

Keep Out Of Reach Of Children.

In case of accidental ingestion, get medical help or contact Poison
Control Center right away. As with any drug, if pregnant or nursing a baby, consult with a doctor before using.