62106-8367 NDC - LYCOPODIUM CLAVATUM (CLUBMOSS)

Drug Information

Product NDC: 62106-8367

Proprietary Name: LYCOPODIUM CLAVATUM

Non Proprietary Name: Clubmoss

Active Ingredient(s):
  • 1 [hp_X]/1 LYCOPODIUM CLAVATUM SPORE


Administration Route(s): ORAL

Dosage Form(s): GRANULE

Labeler Information

Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/20/2015

Package Information

No. Package Code Package Description Billing Unit
162106-8367-410 TUBE in 1 CARTON (62106-8367-4) > 140 GRANULE in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-8367The 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 NAMELYCOPODIUM CLAVATUMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEClubmossThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGRANULEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/20/2015This 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 NAMESeroyal USAName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELYCOPODIUM CLAVATUM SPOREThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1 
ACTIVE INGRED UNIT[hp_X]/1 

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This page was last updated on: 9/13/2019