NDC 69837-510 Sure Result Sr Relief

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:
69837-510
Proprietary Name:
Sure Result Sr Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Brand Management, Llc
Labeler Code:
69837
Start Marketing Date: [9]
03-10-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69837-510-10

Package Description: 1 TUBE in 1 CARTON / 118 g in 1 TUBE (69837-510-09)

Product Details

What is NDC 69837-510?

The NDC code 69837-510 is assigned by the FDA to the product Sure Result Sr Relief which is product labeled by International Brand Management, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69837-510-10 1 tube in 1 carton / 118 g in 1 tube (69837-510-09). 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 Sure Result Sr Relief?

DirectionsRotate pump's spout counter-clockwise slightly to unlock; clockwise to lock.Before using on children under 18 years of age consult a physician.Apply sparingly to affected area not more than 4 times daily. However, for the first use, apply to small area to test for sensitivity or skin reaction.Gently massage into skin until fully absorbed.Wash hands with soap and water thoroughly after each applicationto avoid spreading to the eyes or other sensitive mucous membranes.

Which are Sure Result Sr Relief UNII Codes?

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

Which are Sure Result Sr 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:

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Patient Education

Capsaicin Topical


Topical capsaicin is used to relieve minor pain in muscles and joints caused by arthritis, backaches, muscle strains, bruises, cramps, and sprains. Capsaicin is a substance that is found in chili peppers. It works by affecting nerve cells in the skin that are associated with pain, which results in decreased activity of these nerve cells and a reduced sense of pain.
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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".