NDC 68233-808 Top Medicated Pain Relieving

NDC Product Code 68233-808

NDC CODE: 68233-808

Proprietary Name: Top Medicated Pain Relieving 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

  • 68233 - Albert Max, Inc.

NDC 68233-808-01

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 Pain Relieving with NDC 68233-808 is a product labeled by Albert Max, Inc.. 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: 1875596.

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.

  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)

Product Labeler Information

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

Labeler Name: Albert Max, Inc.
Labeler Code: 68233
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: 12-31-2019 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.

Top Medicated Pain Relieving Product Label Images

Top Medicated Pain Relieving 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 40%

Purpose

External Analgesic

Uses

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

Warnings

For external use onlyDo not use• on wounds • on irritated or damaged skin• otherwise than as directedWhen using this product• avoid contact with the eyes or mucous membranes• do not bandage tightlyStop use and ask a doctor if• condition worsens • symptoms persist for more than 7 days• symptoms clear up and occur again within a few days• excessive irritation of the skin develops• nausea, vomiting, abdominal discomfort, diarrhea, or skin rashes occurs

Directions

• adults and children 12 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 massage as shown in the illustrations. • children under 12 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°C (61° to 86° F) • store in an airtight container

Inactive Ingredients

• Eucalyptus oil • Lavender oil

* Please review the disclaimer below.