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  4. NDC Product Code: 51681-0041 White Flower Strain Relief

NDC 51681-0041 White Flower Strain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51681-0041?
  4. White Flower Strain Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
51681-0041
Proprietary Name:
White Flower Strain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jelma Philippines Inc
Labeler Code:
51681
Product Label ID:
c0d347eb-eab0-4132-874b-0d162b3fe12c
Start Marketing Date: [9]
02-20-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 51681-0041?

The NDC code 51681-0041 is assigned by the FDA to the product White Flower Strain Relief which is product labeled by Jelma Philippines Inc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 51681-0041-1 50 ml in 1 bottle, glass , 51681-0041-2 25 ml in 1 bottle, glass , 51681-0041-3 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 White Flower Strain Relief?

UsesTempoarily relieves minor aches and pains of muscles and joints due to:■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Which are White Flower Strain Relief UNII Codes?

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

Which are White Flower Strain Relief 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 White Flower Strain Relief?

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: 1244943 - camphor 10 % / menthol 15 % / methyl salicylate 50 % Topical Oil
  • RxCUI: 1244943 - camphor 100 MG/ML / menthol 150 MG/ML / methyl salicylate 500 MG/ML Topical Oil

* 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".