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  4. NDC Product Code: 49035-151 Equate Corn And Callus Remover

NDC 49035-151 Equate Corn And Callus Remover

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49035-151?
  5. Equate Corn And Callus Remover 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:
49035-151
Proprietary Name:
Equate Corn And Callus Remover
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores Inc.
Labeler Code:
49035
Product Label ID:
774f4cbc-89d1-4b0d-b8c3-f65ef056507c
Start Marketing Date: [9]
10-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 49035-151?

The NDC code 49035-151 is assigned by the FDA to the product Equate Corn And Callus Remover which is product labeled by Wal-mart Stores Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-151-01 1 bottle, with applicator in 1 box / 9 ml in 1 bottle, with applicator. 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 Equate Corn And Callus Remover?

Wash affected areayou may soak callus or corn in warm water for 5 minutesdry area thoroughly apply one drop at a time to cover each corn or calluslet dryrepeat procedure once or twice daily as needed for up to 14 days (until corn or callus is removed)

Which are Equate Corn And Callus Remover UNII Codes?

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

Which are Equate Corn And Callus Remover 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".