NDC 72968-0004 Herplex
Anatherum Muricatum,Clematis Erecta,Mezereum,Phytolacca Decandra,Ranunculus Bulbosus,Rhus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72968 - Nashco Products Llc
- 72968-0004 - Herplex
Product Characteristics
Product Packages
NDC Code 72968-0004-1
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 72968-0004?
What are the uses for Herplex?
What are Herplex Active Ingredients?
- CHRYSOPOGON ZIZANIOIDES ROOT 12 [hp_X]/1
- CLEMATIS RECTA FLOWERING TOP 12 [hp_X]/1
- DAPHNE MEZEREUM BARK 12 [hp_X]/1
- PHYTOLACCA AMERICANA ROOT 12 [hp_X]/1
- RANUNCULUS BULBOSUS WHOLE 12 [hp_X]/1
- SEPIA OFFICINALIS JUICE 30 [hp_X]/1
- SODIUM CHLORIDE 30 [hp_X]/1 - A ubiquitous sodium salt that is commonly used to season food.
- THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/1
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/1
Which are Herplex UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z)
- CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB)
- RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
Which are Herplex 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM PALMITOSTEARATE (UNII: R4OXA9G5BV)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
* 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".