NDC 69836-2001 Illite Whitening

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

Product Information

Product Code69836-2001
Proprietary Name 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.		Illite Whitening
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		International Nature Soap Institute
Labeler Code69836
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		06-17-2015
Listing Expiration Date 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.		12-31-2018
Exclude Flag 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". 		I
NDC Code Structure

Usage Information


Product Packages

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.

Product Details

Illite Whitening is product labeled by International Nature Soap Institute. The product's dosage form is and is administered via form.


What are Illite Whitening Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)


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)


* Please review the disclaimer below.

Illite Whitening Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



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.