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  4. NDC Product Code: 69176-070 Rapid Gel Rx

NDC 69176-070 Rapid Gel Rx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69176-070?
  4. Rapid Gel Rx 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:
69176-070
Proprietary Name:
Rapid Gel Rx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tmig Inc
Labeler Code:
69176
Product Label ID:
30eb0746-0a66-5874-e054-00144ff8d46c
Start Marketing Date: [9]
04-20-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69176-070?

The NDC code 69176-070 is assigned by the FDA to the product Rapid Gel Rx which is product labeled by Tmig Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69176-070-30 1 tube in 1 carton / 30 ml in 1 tube, 69176-070-90 1 tube in 1 carton / 90 ml 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 Rapid Gel Rx?

Rapid Gel RX is indicated for the relief of pain and inflammation from: arthritis or injuries such as sprains, strains, dislocations, repetitive/overuse injuries, traumatic edema, post-surgical edema, general swelling of joints and soft tissues of the hand, wrist, elbow, shoulder, neck, back, knee, ankle, foot and toe and general aches and pains.

Which are Rapid Gel Rx UNII Codes?

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

Which are Rapid Gel Rx 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".