NDC 66129-134 Dermaclair Skin Lightening

NDC Product Code 66129-134

NDC CODE: 66129-134

Proprietary Name: Dermaclair Skin Lightening 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.

Product Characteristics

Color(s):
WHITE (C48325)

NDC Code Structure

  • 66129 - International Beauty Exchange

NDC 66129-134-31

Package Description: 50 g in 1 TUBE

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

NDC Product Information

Dermaclair Skin Lightening with NDC 66129-134 is a product labeled by International Beauty Exchange. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 199176.

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)
  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • SODIUM METABISULFITE (UNII: 4VON5FNS3C)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Labeler Information

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

Labeler Name: International Beauty Exchange
Labeler Code: 66129
Start Marketing Date: 01-01-2011 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: 12-31-2017 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.

Dermaclair Skin Lightening Product Label Images

Dermaclair Skin Lightening 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

Hydroquinone 2%

Warnings

For external use only

Otc - Do Not Use

On children under 12 years of age unless directed by a doctor

Otc - When Using

Avoid contact with eyes.

Otc - Purpose

Skin Lightener

Indications & Usage

For the gradual fading of dark (brownish) areas in the skin such
as freckles, age and liver spots

Dosage & Administration

Apply a small amount
as a thin layer on the affected area twice daily, or use as directed by a
doctor

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center
right away

Inactive Ingredient

WATER, ALCOHOL, GLYCERIN, CARBOMER COPOLYMER TYPE A, TROLAMINE, SODIUM
METABISULFITE, EDETATE DISODIUM

* Please review the disclaimer below.