Lavender Callus Remover Gel
FDA Label NDC 83691-012

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sansar, Llc for the product Lavender Callus Remover (NDC 83691-012). 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, when using this product, stop use if irritation occurs, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Salicylic acid 12%

Purpose

Corn and callus remover

Uses

  • for the removal of corns and calluses
  • Relieves pain by removing corns and calluses

Warnings

For external use only.

When Using This Product

  • Wear gloves. Limit use to 20 minutes. Use cautiously with electric filing machines.
  • Avoid broken or non calloused skin. 
  • Avoid eye contact. Rinse for 15 minutes if contcat occurs. consult a physician if irritation persists.

Stop Use If Irritation Occurs

Directions

  • Soak feet for 10-15 minutes 
  • Dry with a towel
  • Wear Gloves, apply callus remover gel, leave for 10-15 minutes.
  • Rinse of residue.

Inactive Ingredients

Distilled water, Alcohol ethoxylate, Potassium Hydroxide, Glycerin, Tetrasodium EDTA, Fragrance Essential Oil

* Please review the disclaimer below.