NDC 69836-2001 Illite Whitening

  1. Labeler Index
  2. International Nature Soap Institute
  3. NDC: 69836-2001 Illite Whitening

NDC Product Code 69836-2001

NDC CODE: 69836-2001

Proprietary Name: Illite Whitening What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 69836 - International Nature Soap Institute

NDC 69836-2001-1

Package Description: 100 g in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Illite Whitening with NDC 69836-2001 is a product labeled by International Nature Soap Institute. The generic name of Illite Whitening is . The product's dosage form is and is administered via form.

Labeler Name: International Nature Soap Institute

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • WATER (UNII: 059QF0KO0R)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: International Nature Soap Institute
Labeler Code: 69836
Start Marketing Date: 06-17-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Illite Whitening Product Label Images

Illite Whitening Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling 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.