NDC 73065-0003 Himangchantoothpaste

Precipitated Calcium Carbonate, Aminocaproic Acid, Aluminium Chlorohydrin Allantoinate, Dibasic Calcium Phosphate Hydrate

NDC Product Code 73065-0003

NDC Code: 73065-0003

Proprietary Name: Himangchantoothpaste 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.

Non-Proprietary Name: Precipitated Calcium Carbonate, Aminocaproic Acid, Aluminium Chlorohydrin Allantoinate, Dibasic Calcium Phosphate Hydrate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73065 - Woorilife&health

NDC 73065-0003-1

Package Description: 120 g in 1 TUBE

NDC Product Information

Himangchantoothpaste with NDC 73065-0003 is a a human over the counter drug product labeled by Woorilife&health. The generic name of Himangchantoothpaste is precipitated calcium carbonate, aminocaproic acid, aluminium chlorohydrin allantoinate, dibasic calcium phosphate hydrate. The product's dosage form is paste and is administered via oral form.

Labeler Name: Woorilife&health

Dosage Form: Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Himangchantoothpaste 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.

  • CALCIUM CARBONATE 7.42 g/100g
  • ALCLOXA .06 g/100g

Administration Route(s)

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

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Woorilife&health
Labeler Code: 73065
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: 10-04-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Himangchantoothpaste Product Label Images