50488-2626 NDC - MORCIN (ACONTIUM NAPELLUS)

Drug Information

Product NDC: 50488-2626

Proprietary Name: Morcin

Non Proprietary Name: Acontium Napellus

Active Ingredient(s):
  • 6 [hp_X]/120mL ACHILLEA MILLEFOLIUM;
  • 6 [hp_X]/120mL ACONITUM NAPELLUS;
  • 6 [hp_X]/120mL ARNICA MONTANA;
  • 6 [hp_X]/120mL BELLADONNA LEAF;
  • 6 [hp_X]/120mL BELLIS PERENNIS;
  • 5 [hp_X]/120mL CALENDULA OFFICINALIS FLOWER;
  • 6 [hp_X]/120mL COLCHICUM AUTUMNALE FLOWER;
  • 4 [hp_X]/120mL ECHINACEA ANGUSTIFOLIA;
  • 6 [hp_X]/120mL ECHINACEA PURPUREA;
  • 6 [hp_X]/120mL HAMAMELIS VIRGINIANA WHOLE;
  • 6 [hp_X]/120mL HYPERICUM PERFORATUM;
  • 6 [hp_X]/120mL MATRICARIA RECUTITA


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Labeler Information

Labeler Name: Alexso, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/20/2014

Package Information

No. Package Code Package Description Billing Unit
150488-2626-1120 mL in 1 PACKAGE (50488-2626-1)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC50488-2626The 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 PRESCRIPTION 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 NAMEMorcinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAcontium NapellusThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe 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 DATE3/20/2014This 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 NAMEAlexso, IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACHILLEA MILLEFOLIUM; ACONITUM NAPELLUS; ARNICA MONTANA; BELLADONNA LEAF; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWER; COLCHICUM AUTUMNALE FLOWER; ECHINACEA ANGUSTIFOLIA; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA WHOLE; HYPERICUM PERFORATUM; MATRICARIA RECUTITAAn 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 STRENGTH6; 6; 6; 6; 6; 5; 6; 4; 6; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL; [hp_X]/120mL 

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