66096-726 NDC - DAMIANA COMPLEX (AGNES CASTUS, AVENA SATIVA, DAMIANA, GELSEMIUM SEMPERVIRENS, IGNATIA AMARA, LYCOPODIUM CLAVATUM, ORCHITINUM, PHOSPHORICUM ACIDUM, SABAL SERRULATA, SELENIUM METALLICUM.)

Drug Information

Product NDC: 66096-726

Proprietary Name: Damiana Complex

Non Proprietary Name: Agnes Castus, Avena Sativa, Damiana, Gelsemium Sempervirens, Ignatia Amara, Lycopodium Clavatum, Orchitinum, Phosphoricum Acidum, Sabal Serrulata, Selenium Metallicum.

Active Ingredient(s):
  • 3 [hp_X]/59mL AVENA SATIVA FLOWERING TOP;
  • 3 [hp_X]/59mL CHASTE TREE;
  • 12 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT;
  • 12 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/59mL PHOSPHORIC ACID;
  • 3 [hp_X]/59mL SAW PALMETTO;
  • 12 [hp_X]/59mL SELENIUM;
  • 12 [hp_X]/59mL STRYCHNOS IGNATII SEED;
  • 12 [hp_X]/59mL SUS SCROFA TESTICLE;
  • 3 [hp_X]/59mL TURNERA DIFFUSA LEAFY TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: OHM PHARMA INC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/19/2015

Package Information

No. Package Code Package Description Billing Unit
166096-726-0559 mL in 1 BOTTLE, SPRAY (66096-726-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC66096-726The 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 NAMEDamiana ComplexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAgnes Castus, Avena Sativa, Damiana, Gelsemium Sempervirens, Ignatia Amara, Lycopodium Clavatum, Orchitinum, Phosphoricum Acidum, Sabal Serrulata, Selenium Metallicum.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE8/19/2015This 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 NAMEOHM PHARMA INC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAVENA SATIVA FLOWERING TOP; CHASTE TREE; GELSEMIUM SEMPERVIRENS ROOT; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; SAW PALMETTO; SELENIUM; STRYCHNOS IGNATII SEED; SUS SCROFA TESTICLE; TURNERA DIFFUSA LEAFY TWIGAn 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 STRENGTH3; 3; 12; 12; 12; 3; 12; 12; 12; 3 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 

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