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  4. NDC Product Code: 62936-0042 Laura Lynn Anticavity Whitening Plus Mouthwash

NDC 62936-0042 Laura Lynn Anticavity Whitening Plus Mouthwash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62936-0042?
  5. Laura Lynn Anticavity Whitening Plus Mouthwash Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62936-0042
Proprietary Name:
Laura Lynn Anticavity Whitening Plus Mouthwash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ingles Market Inc
Labeler Code:
62936
Product Label ID:
bb1e1a54-f421-4824-a9a2-eb375ecd342d
Start Marketing Date: [9]
08-29-2003
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
MINT (C73404 - MINTY FRESH)

Code Structure Chart

Product Details

What is NDC 62936-0042?

The NDC code 62936-0042 is assigned by the FDA to the product Laura Lynn Anticavity Whitening Plus Mouthwash which is product labeled by Ingles Market Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62936-0042-5 181.4 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 Laura Lynn Anticavity Whitening Plus Mouthwash?

Adults and children         Brush teeth thoroughly, preferably after2 years and older            each meal, or at least twice a day, or as                                         directed by your dentist.  Do not swallow.Children under                 To minimize swallowing, use a pea-6 years of age                 sized amount and supervise brushing                                          until good habits are established.Children under 2 years  Ask a dentist or physician.

Which are Laura Lynn Anticavity Whitening Plus Mouthwash UNII Codes?

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

Which are Laura Lynn Anticavity Whitening Plus 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:

What is the NDC to RxNorm Crosswalk for Laura Lynn Anticavity Whitening Plus Mouthwash?

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: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste

* 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".