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  4. NDC Product Code: 10237-773 Orajel Fluoride

NDC 10237-773 Orajel Fluoride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10237-773?
  5. Orajel Fluoride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10237-773
Proprietary Name:
Orajel Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Church & Dwight Co., Inc.
Labeler Code:
10237
Product Label ID:
5c4ff036-711a-373a-e053-2a91aa0a756a
Start Marketing Date: [9]
10-24-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Flavor(s):
BERRY (C73365 - BUBBLE BERRY)

Product Packages

NDC Code 10237-773-42

Package Description: 1 g in 1 TUBE

Product Details

What is NDC 10237-773?

The NDC code 10237-773 is assigned by the FDA to the product Orajel Fluoride which is product labeled by Church & Dwight Co., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10237-773-42 1 g in 1 tube . 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 Orajel Fluoride?

Twist off cap and remove foil sealdo not swallowsupervise children as necessary until capable of using without supervisionadults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physicianchildren under 6 years: instruct in good brushing and rinsing habits (to minimize swallowing)children under 2 years: ask a dentist or physician

Which are Orajel Fluoride UNII Codes?

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

Which are Orajel Fluoride 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:

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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".