73296-012 NDC - GELSEMIUM SEMPERVIRENS, NUX MOSCHATA, AVENA SATIVA, ESCHSCHOLTZIA CALIFORNICA, PASSIFLORA INCARNATA, PIPER METHYSTICUM, VALERIANA OFFICINALIS, CHAMOMILLA

Drug Information

  • Product NDC: 73296-012
  • Proprietary Name:
  • Non Proprietary Name: Gelsemium sempervirens, Nux moschata, Avena sativa, Eschscholtzia californica, Passiflora incarnata, Piper methysticum, valeriana officinalis, Chamomilla
  • Active Ingredient(s): 6 [hp_X]/12kg ALFALFA; 6 [hp_X]/12kg AVENA SATIVA FLOWERING TOP; 6 [hp_X]/12kg ESCHSCHOLZIA CALIFORNICA; 12 [hp_X]/12kg GELSEMIUM SEMPERVIRENS ROOT; 6 [hp_X]/12kg MATRICARIA CHAMOMILLA; 9 [hp_X]/12kg NUTMEG; 6 [hp_X]/12kg PASSIFLORA INCARNATA TOP; 6 [hp_X]/12kg PIPER METHYSTICUM ROOT; 6 [hp_X]/12kg VALERIAN
  • Administration Route(s):
  • Dosage Form(s): POWDER

Labeler Information

Field Name Field Value
Labeler Name: Laboratoire Schmidt-Nagel
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:9/17/2019

Package Information

No. Package Code Package Description Billing Unit
173296-012-101 BAG in 1 PAIL (73296-012-10) / 10 kg in 1 BAG

NDC Record

Field Name Field Value Definition
PRODUCT NDC73296-012The 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 NAMEDRUG FOR FURTHER PROCESSINGIndicates 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.
NON PROPRIETARY NAMEGelsemium sempervirens, Nux moschata, Avena sativa, Eschscholtzia californica, Passiflora incarnata, Piper methysticum, valeriana officinalis, ChamomillaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDERThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE9/17/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGProduct 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 NAMELaboratoire Schmidt-NagelName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALFALFA; AVENA SATIVA FLOWERING TOP; ESCHSCHOLZIA CALIFORNICA; GELSEMIUM SEMPERVIRENS ROOT; MATRICARIA CHAMOMILLA; NUTMEG; PASSIFLORA INCARNATA TOP; PIPER METHYSTICUM ROOT; VALERIANAn 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; 12; 6; 9; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg; [hp_X]/12kg 

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This page was last updated on: 12/6/2025