Herplex Tablet
NDC Package 72968-0002-1
Package Information
Herplex (anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia) tablets is 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. This formulation utilizes a tablet delivery system. Marketed by Nashco Products Llc, this product is identified by NDC 72968-0002.
Identification & Billing
Clinical Specifications
- 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
- THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/1
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/1
Regulatory & Marketing
Hierarchy Structure
- 72968 - Nashco Products Llc
- 72968-0002 - Herplex
- 72968-0002-1 - 60 TABLET in 1 BOTTLE, PLASTIC
- 72968-0002 - Herplex
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 72968-0002-1 identifies a specific commercial package of 60 tablet in 1 bottle, plastic of Herplex, a human over the counter drug labeled by Nashco Products Llc. This tablet is formulated for oral use and contains 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 as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Nashco Products Llc on April 18, 2019.
How is this Nashco Products Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72968000201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.