NDC 41250-703 Oral Analgesic Maximum Strength

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:
41250-703
Proprietary Name:
Oral Analgesic Maximum Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meijer Distribution Inc.
Labeler Code:
41250
Start Marketing Date: [9]
05-13-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41250-703-45

Package Description: 1 BOTTLE, GLASS in 1 CARTON / 13.3 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 41250-703?

The NDC code 41250-703 is assigned by the FDA to the product Oral Analgesic Maximum Strength which is product labeled by Meijer Distribution Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41250-703-45 1 bottle, glass in 1 carton / 13.3 ml in 1 bottle, glass. 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 Analgesic Maximum Strength?

Directions   remove imprinted safety seal from bottle capAdults and children 2 years of age and over                  Apply product with cotton swab or clean fingertip to the affected area.                                                                                 Use up to 4 times daily or as directed by a dentist or doctorChildren under 12 years of age                                     Should be supervised in the use of this productChildren under 2 years of age                                       Ask a dentist or doctorOther information do not use if imprinted bottle seal is broken or missing prior to opening

Which are Oral Analgesic Maximum Strength UNII Codes?

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

Which are Oral Analgesic Maximum Strength 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:

What is the NDC to RxNorm Crosswalk for Oral Analgesic Maximum Strength?

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:
  • RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
  • RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution

* 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".