NDC 42681-0036 365 Whole Foods Market Anticavity/antigingivitis Mouthwash

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:
42681-0036
Proprietary Name:
365 Whole Foods Market Anticavity/antigingivitis Mouthwash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Whole Foods Market, Inc.
Labeler Code:
42681
Start Marketing Date: [9]
01-31-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
SPEARMINT (C73416)

Product Packages

NDC Code 42681-0036-1

Package Description: 946 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 42681-0036?

The NDC code 42681-0036 is assigned by the FDA to the product 365 Whole Foods Market Anticavity/antigingivitis Mouthwash which is product labeled by Whole Foods Market, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42681-0036-1 946 ml in 1 bottle, plastic . 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 365 Whole Foods Market Anticavity/antigingivitis Mouthwash?

Uses • Aids in the prevention of dental cavities. • Helps remove plaque that leads to gingivitis, an early form of gum disease. • The combined daily use of a fluoride preventative treatment rinse and a fluoride toothpaste can help reduce the incidence of dental cavities.

Which are 365 Whole Foods Market Anticavity/antigingivitis Mouthwash UNII Codes?

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

Which are 365 Whole Foods Market Anticavity/antigingivitis Mouthwash 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".