Botanimedix Tinearx Antifungal Drying Emulsion
FDA Label NDC 52261-5801

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cosco International, Inc. for the product Botanimedix Tinearx Antifungal Drying Emulsion (NDC 52261-5801). 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 drug facts, uses:, indications & usage, directions:, warnings:, otc - keep out of reach of children, inactive ingredients:, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient                          Purpose
Clotrimazole 1%........................Anti-fungal

Uses:

Cures most athlete's foot, jock itch, and ring worm

Indications & Usage

For relief of:

  • Itching, burning, cracking, scaling, and discomfort which accompany these conditions.

Directions:

Apply twice daily for best results.

Warnings:

For external use only.

When using this product

  • Do not get into eyes.
  • Stop use and ask a doctor if:

    • Condition worsens.
    • Symptoms last more than 7 days or clear and occur again within a few days. 

Otc - Keep Out Of Reach Of Children

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

Inactive Ingredients:

Aluminum Starch Octenylsuccinate, Cannabidiol, Clove Leaf Oil, Dipropylene Glycol, Eucalyptus Oil, Glyceryl Monostearate, Hypromellose, Isopropyl Myristate, Isopropyl Palmitate, Peppermint Oil, Phenoxyethanol, Ethylhexylglycerin, Polyoxyl 20 Cetostearyl Ether, Tea Tree Oil, Water

Questions?

Call:  1-800-964-5406

www.botanimedix.com

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