NDC 72531-100 Doctor Will

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72531-100
Proprietary Name:
Doctor Will
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yirrh Healthy Living Company
Labeler Code:
72531
Start Marketing Date: [9]
09-17-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 72531-100-02

Package Description: 1 TUBE in 1 CARTON / 150 g in 1 TUBE (72531-100-01)

Product Details

What is NDC 72531-100?

The NDC code 72531-100 is assigned by the FDA to the product Doctor Will which is product labeled by Yirrh Healthy Living Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72531-100-02 1 tube in 1 carton / 150 g in 1 tube (72531-100-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Doctor Will?

Adults and children 2 years of age and olderBrush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.Children 2 to 6 yearsUse only a pea sized amount and supervise child’s brushing and rinsing (to minimize swallowing).Children under 2 yearsAsk a dentist or physician

Which are Doctor Will UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Doctor Will Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".