NDC 62040-1001 Eco Whitening

NDC Product Code 62040-1001

NDC CODE: 62040-1001

Proprietary Name: Eco 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.

NDC Code Structure

NDC 62040-1001-2

Package Description: 3 BOTTLE, PLASTIC in 1 PACKAGE > 2 mL in 1 BOTTLE, PLASTIC (62040-1001-1)

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

NDC Product Information

Eco Whitening with NDC 62040-1001 is a product labeled by Jn Pharm. The product's dosage form is and is administered via form.

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)

Product Labeler Information

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

Labeler Name: Jn Pharm
Labeler Code: 62040
Start Marketing Date: 02-08-2014 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.

Eco Whitening Product Label Images

Eco 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

Hydrogen Peroxide

Inactive Ingredient

Polyvinylpyrrolidone, Ethanol, Glycerin, Dipotassium Glycyrrhizate, Polyoxyethylene Hydrogenated Castor Oil, Methylparaben, sodium Saccharin, Mentha oil, Purified water

Otc - Purpose

Teeth whitening

Otc - Keep Out Of Reach Of Children

Keep out or reach of the children

Indications & Usage

-After getting rid of excess moisture on your teeth, apply a suitable amount of gel onto your teeth. -Do not close your mouth until the gel is completely dried. (It takes about 30~60sec until it is evaporated).-Rinse out with water after 30 minutes. -Twice a day(in the morning and the evening), do the followings for two weeks


*Be careful if you are with these troubles below.-Allergic to hydrogen peroxide-Infection in the mouth, damages on your teeth, gum diseases-Teeth Calibration in progress*Specific Caution : -If you have a toothache, reduce the usage to once a day. If your toothache lasts   longer, stop using it for 2~3 days and start using it again. -If gum diseases or intraoral troubles, stop using it.-If you have a toothache continuously, then go to see a dentist.-Use the appropriate amount of the product.-Do not swallow.-In case of accidental ingestion, seek professional assistance.-When pregnant or lactating women use the product, check with a doctor before    using it.-In case of the usage by kids under 12 years of age, seek for professional assistance first.-While the gel is applied onto your teeth, do not eat, drink, smoke, or wash your face.- Be careful not to make clothes to be stained with the gel.

Dosage & Administration

Dental use only

* Please review the disclaimer below.