NDC 0041-1421 Oral-b Anticavity

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:
Proprietary Name:
Oral-b Anticavity
Product Type: [3]
Labeler Name: [5]
Oral-b Laboratories
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Characteristics

BLUE (C48333)
MINT (C73404)

Product Packages

NDC Code 0041-1421-16

Package Description: 500 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 0041-1421?

The NDC code 0041-1421 is assigned by the FDA to the product Oral-b Anticavity which is product labeled by Oral-b Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0041-1421-16 500 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 Oral-b Anticavity?

Adults and children 6 years and older: use once a day after brushing your teeth with toothpaste.Vigorously swish 10ml (as indicated inside cap) of rinse between your teeth for 1 minute then spit out. Do not swallow.Do not eat or drink for 30 minutes after rinsing.Instruct children under 12 years of age in good rinsing habits to minimize swallowing.Supervise children as necessary until capable of using without supervision.Consult a dentist or physician for use by children under 6 years of age.

Which are Oral-b Anticavity UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Oral-b Anticavity?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".