Illite Whitening
FDA Label NDC 69836-2001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by International Nature Soap Institute for the product Illite Whitening (NDC 69836-2001). 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 - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

glycerine


Inactive Ingredient

coconut oil, palm oil, olive oil, sodium hydroxide, water, lavender, etc


Otc - Purpose

skin protectant


Otc - Keep Out Of Reach Of Children

keep out of reach of the children

Indications & Usage

apply to the skin and wash away


Warnings

・Stop using the product when you have skin problems or the product disagrees with your skin
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・If the product gets into the eyes, don't rub but rinse with water.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.


Dosage & Administration

for external use only

* Please review the disclaimer below.