NDC 24438-001 Phoenix Balm

NDC Product Code 24438-001

NDC CODE: 24438-001

Proprietary Name: Phoenix Balm 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

  • 24438 - Amazonian Naturals, Inc.

NDC 24438-001-02

Package Description: 1 CONTAINER in 1 BOX > 19 g in 1 CONTAINER (24438-001-01)

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

NDC Product Information

Phoenix Balm with NDC 24438-001 is a product labeled by Amazonian Naturals, 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: 1232398.

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.

  • CAT'S CLAW (UNII: 9060PRM18Q)

Product Labeler Information

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

Labeler Name: Amazonian Naturals, Inc.
Labeler Code: 24438
Start Marketing Date: 12-01-2011 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: 12-31-2017 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.

Phoenix Balm 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 5%.................................... Topical AnalgesicMenthol 5% ..................................... Topical AnalgesicMethyl Salicylate 5%........................ Topical Analgesic


Topical Analgesic


For temporary relief of minor aches and pains of muscles and joints associated with over-exertions, arthritis, strains and sprains.


Warnings    For external use only.

When Using This Product

  • Avoid contact with eyes and mucous membranes.Do not apply to open wounds or damaged skin.Do not bandage or use heating pad.

Stop Use And Ask A Doctor If

  • Condition Worsens.Severe skin irritation occurs.Pain persists for more than seven days.Pain clears up and then recurs a few days later.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding ask a health care professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.  If swallowed get medical help or contact a Poisen Control Center immediately.


  • Rub well on the affected area.  Repeat 2 or 3 times daily.For children 2 - 12 years, consult a doctor before use.

Other Information

This product may cause allergic reaction in some people.  Test on small area before use.

Inactive Ingredients

Pine needle oil, Cats Claw and Paraffin Petrolatum

* Please review the disclaimer below.