Cureforte Anti Fungal Foot Care Liquid
FDA Label NDC 85884-252

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Steel City Health Private Limited for the product Cureforte Anti Fungal Foot Care (NDC 85884-252). 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 otc - purpose, otc - keep out of reach of children, warnings, dosage & administration, indications & usage, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Otc - Purpose

→ Otc - Keep Out Of Reach Of Children

→ Warnings

→ Dosage & Administration

→ Indications & Usage

→ Inactive Ingredient

→ Package Label.principal Display Panel

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