NDC 72968-0002 Herplex

Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia

NDC Product Code 72968-0002

NDC Code: 72968-0002

Proprietary Name: Herplex What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia 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.

NDC Code Structure

  • 72968 - Nashco Products Llc
    • 72968-0002 - Herplex

NDC 72968-0002-1

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

NDC Product Information

Herplex with NDC 72968-0002 is a a human over the counter drug product labeled by Nashco Products Llc. The generic name of Herplex is anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Nashco Products Llc

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug 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.

Herplex Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • 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 12 [hp_X]/1
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/1
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/1
  • SODIUM CHLORIDE 30 [hp_X]/1
  • SEPIA OFFICINALIS JUICE 30 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nashco Products Llc
Labeler Code: 72968
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 04-18-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Herplex Product Label Images

Herplex Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Anatherum Muricatum 12X, Clematis Erecta 12X, Mezereum 12X, Phytolacca Decandra 12X, Ranunculus Bulbosus 12X, Rhus Tox 12X, Thuja Occidentalis 12X, Natrum Muriaticum 30X, Sepia 30X.

Uses:

Herplex can be used for temporarily relieving outbreaks of cold sores and genital herpes.

Herplex can be used for temporarily relieving outbreaks of cold sores and genital herpes.

Warnings:

Do not use unless you have been diagnosed by a physician with oral herpes or genital herpes.CAUTION: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Not recommended for children under 12.If you are pregnant or breast-feeding, ask your doctor before use.TAMPER EVIDENT: DO NOT USE IF IMPRINTED SHRINK SEAL AROUND NECK AND CAP IS BROKEN OR MISSING.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

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.

Inactive Ingredients:

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

Package Label Display:

>ORAL HERPES/COLD SORES>GENITAL HERPESHERPLEXA New Beginning•Safe •Non-prescription•Homeopathic60 TABLETS

* Please review the disclaimer below.

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