NDC 33261-884 Medrox

NDC Product Code 33261-884

NDC CODE: 33261-884

Proprietary Name: Medrox What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 33261 - Aidarex Pharmaceuticals Llc

NDC 33261-884-01

Package Description: 5 PATCH in 1 BOX > 10 g in 1 PATCH

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Medrox with NDC 33261-884 is a product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1300889.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Aidarex Pharmaceuticals Llc
Labeler Code: 33261
Start Marketing Date: 06-13-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Medrox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Menthol                     5.00%Capsaicin                  0.0375%


Analgesic/CounterirritantExternal Analgesic


Use for the temporary relief of minor aches and muscle pains associated with arthritis, simple backache, strains, muscle soreness and stiffness.


  • For external use only. Use only as directed. Avoid contact with eyes and mucous membranes.Do not cover with bandage.Do not use on wounds or damaged skin.Consult physician for  children under 12.Do not use if you are allergic to MentholStop use and ask a doctor if conditions worsen, symptoms persist for more than 7 days or clear up and occur again within a few daysOr rash, itching or excessive skin irritation occurs.


  • Adults and children 12 years and over apply to affected area: change patch 1 to 2 times dailyChildren under 12 years, consult physician before useHow to apply:Clean and dry affected areaCut open pouch and remove patchRemove protective film and apply directly to area of painApply to affected area not more than 3 times dailyWash hands with soap after applying patchReseal pouch containing unused patches

Other Ingredients

Water, Glycerine, Sodium Polyacrylate, Polysorbate 80, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, EDTA Disodiumm Salt, Diazolidinyl Urea, Methylparaben, Iodoproynyl Butylcabamate, Propylparaben.

* Please review the disclaimer below.