NDC 66096-721 Ohm-dam
Agnus Castus,Avena Sativa,Damiana,Gelsemium Sempervirens,Ignatia Amara,Lycopodium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66096 - Ohm Pharma Inc.
- 66096-721 - Ohm-dam
Product Packages
NDC Code 66096-721-02
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 66096-721?
What are Ohm-dam Active Ingredients?
- AVENA SATIVA FLOWERING TOP 5 [hp_X]/30mL
- BOS TAURUS TESTICLE 12 [hp_X]/30mL
- CHASTE TREE FRUIT 5 [hp_X]/30mL
- GELSEMIUM SEMPERVIRENS ROOT 14 [hp_X]/30mL
- LYCOPODIUM CLAVATUM SPORE 14 [hp_X]/30mL
- PHOSPHORIC ACID 14 [hp_X]/30mL
- SAW PALMETTO 5 [hp_X]/30mL
- SELENIUM 12 [hp_X]/30mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
- STRYCHNOS IGNATII SEED 14 [hp_X]/30mL
- TRIBULUS TERRESTRIS WHOLE 7 [hp_X]/30mL
- TURNERA DIFFUSA LEAFY TWIG 5 [hp_X]/30mL
- YOHIMBINE 10 [hp_X]/30mL - A plant alkaloid with alpha-2-adrenergic blocking activity. Yohimbine has been used as a mydriatic and in the treatment of ERECTILE DYSFUNCTION.
Which are Ohm-dam UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- BOS TAURUS TESTICLE (UNII: PR4RXL6G2H)
- BOS TAURUS TESTICLE (UNII: PR4RXL6G2H) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT)
- TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT) (Active Moiety)
- YOHIMBINE (UNII: 2Y49VWD90Q)
- YOHIMBINE (UNII: 2Y49VWD90Q) (Active Moiety)
Which are Ohm-dam Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An 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.
[3] What kind of product is this? - Indicates 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".