62400-0055 NDC - MAGNILIFE KNEE PAIN RELIEF GEL (ARNICA MONTANA FLOWER, TOXICODENDRON PUBESCENS LEAF)

Drug Information

Product NDC: 62400-0055

Proprietary Name: Magnilife Knee pain relief gel

Non Proprietary Name: ARNICA MONTANA FLOWER, TOXICODENDRON PUBESCENS LEAF

Active Ingredient(s):
  • 1 [hp_X]/g ARNICA MONTANA FLOWER;
  • 4 [hp_X]/g TOXICODENDRON PUBESCENS LEAF


Administration Route(s): TOPICAL

Dosage Form(s): GEL

Labeler Information

Labeler Name: United Laboratories Manufacturing, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/10/2022

Package Information

No. Package Code Package Description Billing Unit
162400-0055-1113 g in 1 JAR (62400-0055-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62400-0055The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEMagnilife Knee pain relief gelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEARNICA MONTANA FLOWER, TOXICODENDRON PUBESCENS LEAFThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGELThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/10/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEUnited Laboratories Manufacturing, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARNICA MONTANA FLOWER; TOXICODENDRON PUBESCENS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1; 4 
ACTIVE INGRED UNIT[hp_X]/g; [hp_X]/g 

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This page was last updated on: 2/1/2023