Herplex Tablet
NDC 72968-0002

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72968-0002?
  5. Herplex Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

Herplex (anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nashco Products Llc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a white tablet for oral administration. This product entry covers the primary NDC 72968-0002 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
72968-0002
Proprietary Name:
Herplex
Non-Proprietary Name: [1]
Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia
Substance Name: [2]
Chrysopogon Zizanioides Root; Clematis Recta Flowering Top; Daphne Mezereum Bark; Phytolacca Americana Root; Ranunculus Bulbosus Whole; Sepia Officinalis Juice; Sodium Chloride; Thuja Occidentalis Leafy Twig; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Nashco Products Llc
Labeler Code:
72968
Product Label ID:
fad9615f-7004-415d-9f69-ee9ff95f0067
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
04-18-2019
End Marketing Date: [10]
12-28-2026
Exclude Flag: [12]
N

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
DIAMOND
Score:
1

Code Structure Chart

Product Details

What is NDC 72968-0002?

The NDC code 72968-0002 is assigned by the FDA to the product Herplex. It is commonly known by its generic name, anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia. This pharmaceutical product is labeled by Nashco Products Llc and is currently categorized as listed product. The medication is a tablet administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 72968-0002-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

For use only after diagnoses by a physician, as follows:Cold Sores/Oral Herpes: Take 3 tablets immediately at the first sign of burning or itching and then 3 tablets three times daily until symptoms disappear.Genital Herpes: For severe genital herpes sufferers, take 3 to 5 tablets 3 times daily for prevention of outbreaks. If you have an outbreak that does not subside within 10 days, consult your doctor. For mild to moderate symptoms, take 3 tablets immediately at the first sign of burning or itching, and then 3 tablets three times daily until symptoms disappear. If symptoms do not subside within 10 days, consult your doctor.

What are Active Ingredients of this product?

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.

Which are the associated 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 (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)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)

Which are the Inactive Ingredients associated 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:

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the End Marketing Date? This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".