NDC 50943-001 Top Medicated

NDC Product Code 50943-001

NDC CODE: 50943-001

Proprietary Name: Top Medicated 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

  • 50943 - A&a Medical Supplies

NDC 50943-001-01

Package Description: 50 mL in 1 BOTTLE

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

NDC Product Information

Top Medicated with NDC 50943-001 is a product labeled by A&a Medical Supplies. 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: 1193297.

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.

  • CLOVE OIL (UNII: 578389D6D0)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • TURPENTINE OIL (UNII: C5H0QJ6V7F)

Product Labeler Information

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

Labeler Name: A&a Medical Supplies
Labeler Code: 50943
Start Marketing Date: 05-24-2012 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: 12-31-2018 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.

Top Medicated 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

Camphor 10%Menthol 16%Methyl Salicylate 50%

Purpose

External Analgesic

Uses

  • Temporarily relieves minor aches and pains of muscles and joints due to:simple backachestrainsbruisesarthritissprains

Warnings

For external use only

Otc - Do Not Use

  • Do not useon woundson irritated or damaged skinotherwise than as directed

Otc - When Using

  • When using this productavoid contact with the eyes or mucous membranesdo not bandage tightly

Otc - Stop Use

  • Stop use and ask a doctor if:condition worsenssymptoms persist for more than 7 dayssymptoms clear up and occur again within a few daysexcessive irritation of the skin developsnausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenIF swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 3 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 to 2 times daily. After applying the product, a warm pad may be placed on the affected area for 10 minutes and then massaged as shown in the illustrations.children under 3 years of age: consult your physician.refer to the above warnings; use otherwise than as directed may be dangerous.

Other Information

  • Store at 16 to 30 degrees C (16 to 86 degrees F)preserve in tight container

Inactive Ingredients

  • Clove OilLavender OilTurpentine Oil

* Please review the disclaimer below.