NDC 23636-1001 Nbf Gingival

NDC Product Code 23636-1001

NDC CODE: 23636-1001

Proprietary Name: Nbf Gingival 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

  • 23636 - Nanocuretech

NDC 23636-1001-1

Package Description: 30 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

Nbf Gingival with NDC 23636-1001 is a product labeled by Nanocuretech. 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.

  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • TRICLOSAN (UNII: 4NM5039Y5X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SORBITOL (UNII: 506T60A25R)
  • CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • PROPOLIS WAX (UNII: 6Y8XYV2NOF)
  • XYLITOL (UNII: VCQ006KQ1E)
  • SACCHARIN SODIUM (UNII: SB8ZUX40TY)
  • MENTHA PIPERITA (UNII: 79M2M2UDA9)
  • MENTHOL (UNII: L7T10EIP3A)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • 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: Nanocuretech
Labeler Code: 23636
Start Marketing Date: 11-11-2011 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.

Nbf Gingival Product Label Images

Nbf Gingival 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

Active ingredient: sodium monofluorophosphate

Inactive Ingredient

Inactive ingredient: silicon dioxide, triclosan, glycerin, d-sorbitol, polyethylene glycol, chitosan oligosaccharide, carboxymethylcellulose sodium, propolis extract, xylitol, sacccharin sodium hydroate, peppermint oil, l-menthol, sodium benzoate, ascorbic acid, tocopherol, purified water

Otc - Purpose

■ prevention of gingival disease

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Apply toothpast on soft bristle toothbrush and brush

Warnings

If irritation occurs when using this product, discontinue use

Dosage & Administration

■ apply three times a day after meals

* Please review the disclaimer below.