NDC 72800-004 Extra Strength Joint And Muscle Relief 1500 Mg

NDC Product Code 72800-004

NDC CODE: 72800-004

Proprietary Name: Extra Strength Joint And Muscle Relief 1500 Mg 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

  • 72800 - Lifecure Rx Specialty Pharmacy
    • 72800-004 - Extra Strength Joint And Muscle Relief 1500 Mg

NDC 72800-004-50

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

Extra Strength Joint And Muscle Relief 1500 Mg with NDC 72800-004 is a product labeled by Lifecure Rx Specialty Pharmacy. 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: 2119808.

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.

  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • CARBOMER 934 (UNII: Z135WT9208)
  • JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
  • HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
  • ALCOHOL (UNII: 3K9958V90M)
  • GERANIUM THUNBERGII FLOWERING TOP (UNII: 9IXM1668B6)
  • HEMP (UNII: TD1MUT01Q7)
  • HORSE CHESTNUT (UNII: 3C18L6RJAZ)
  • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • OLEIC ACID (UNII: 2UMI9U37CP)
  • 1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: 7L874P1M1O)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Lifecure Rx Specialty Pharmacy
Labeler Code: 72800
Start Marketing Date: 03-05-2019 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: 12-31-2020 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.

Extra Strength Joint And Muscle Relief 1500 Mg Product Label Images

Extra Strength Joint And Muscle Relief 1500 Mg 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

Uses

Temporary relief of minor arthritis, backache, muscle and joint pain

Warnings

For external use onlyAllergy alert: If prone to allergic reaction to latex, consult a doctor before use. Symptoms may include: • rash • blisters • skin reddeningIf a skin reaction occurs, stop use and seek medical help right away.

Directions

• adults and children 12 and older: Apply 1 to 4 pumps to areas of pain and discomfort. Reapply as necessary using no more than 4 times daily.• children under the age of 12: Do not use, ask a doctor

When Using This Product:

• Use only as directed • Avoid contact with eyes and mucous membranes • do not use with a heating pad • do not bandage tightly • do not apply to wounds or damaged skin

Stop And Ask Doctor If

• condition worsens • symptoms last for more than 7 days • symptoms clear up and occur again within a few days • redness or irritation occurs

Storage

• Store at 20-35 deg C (68-77deg F).

Keep Out Of Reach Of Children And Pets

If swallowed, get medical help or contact poison control right away.

Active Ingredients & Purpose

Menthol 4%----------------- AnalgesicLidocaine 3%--------------- Analgesic

Inactive Ingredient

Bergamot oil, carbomer 940, caderwood oil, devil' claw extract, ethanol, geranium oil, Glydant Plus, hemp extract cannabidiol oil, horse chestnut seed extract, lavender oil, oleic acid, propylene glycol, purified water, soya photidylcholine, triethanolamine.

* Please review the disclaimer below.