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  4. NDC Product Code: 51121-035 Burnaid Burn Gel

NDC 51121-035 Burnaid Burn Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51121-035?
  4. Burnaid Burn Gel Uses
  5. Active Ingredients UNII Codes
  6. 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:
51121-035
Proprietary Name:
Burnaid Burn Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clear Healthcare Llc
Labeler Code:
51121
Product Label ID:
a44e6c9f-02d0-4c70-9daa-759540ef9841
Start Marketing Date: [9]
11-04-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 51121-035?

The NDC code 51121-035 is assigned by the FDA to the product Burnaid Burn Gel which is product labeled by Clear Healthcare Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51121-035-04 115 g in 1 bottle, plastic , 51121-035-12 3.5 g in 1 packet . 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 Burnaid Burn Gel?

1. Tear open sachet. 2. Apply gel liberally to affected area. Do not rub in. 3. Cover if necessary.4. Seek medical attention if pain persists.

Which are Burnaid Burn Gel UNII Codes?

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

Which are Burnaid Burn Gel 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".