NDC 70602-003 Exoden Powder

Cetylpyridinium Chloride, Domiphen Bromide

NDC Product Code 70602-003

NDC 70602-003-02

Package Description: 1 POUCH in 1 CARTON > 10 g in 1 POUCH (70602-003-01)

NDC 70602-003-04

Package Description: 1 CONTAINER in 1 CARTON > 30 g in 1 CONTAINER (70602-003-03)

NDC 70602-003-06

Package Description: 1 CONTAINER in 1 CARTON > 70 g in 1 CONTAINER (70602-003-05)

NDC Product Information

Exoden Powder with NDC 70602-003 is a a human over the counter drug product labeled by Lifeon Corp.. The generic name of Exoden Powder is cetylpyridinium chloride, domiphen bromide. The product's dosage form is powder and is administered via topical form.

Labeler Name: Lifeon Corp.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Exoden Powder Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • DOMIPHEN BROMIDE .12 1/100g

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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Lifeon Corp.
Labeler Code: 70602
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-09-2021 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: 12-31-2022 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: N - NO 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.

Exoden Powder Product Label Images

Exoden Powder 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

Cetylpyridinium Chloride(CPC) 0.43%

Domiphen Bromide 0.120

Otc - Purpose

Oral Health Care

Indications & Usage

Provide better health to teeth and gums

Dosage & Administration

Wet your toothbrush, shake off surplus water and press into powder. Brush teeth thoroughly and rinse


Ask a dentist before use if you have

• bleeding or redness lasting more than 2 weeks

• pain, swelling, pus, loose teeth, or more spacing between teeth

These may be signs of periodontitis, a serious form of gum disease

Otc - Keep Out Of Reach Of Children

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

Inactive Ingredient

Bentonite, Sodium Chloride(Bamboo Salts), L-Menthol

* Please review the disclaimer below.