Herpeset Spray
NDC Package 50845-0126-1
Package Information
Herpeset (apis mellifica, arsenicum album, baptisia tinctoria, capsicum annuum, dulcamara, echinacea, nitricum acidum, pyrogenium, rhus toxicodendron,) sprays is iNDICATIONS: Relieves symptoms associated with the cold sores: oral eruptions, swelling, skin eruptions and discomfort. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0126.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories, Inc.
- 50845-0126 - Herpeset
- 50845-0126-1 - 30 mL in 1 BOTTLE, SPRAY
- 50845-0126 - Herpeset
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.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 50845-0126-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Herpeset, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains apis mellifera; arsenic trioxide; baptisia tinctoria root; capsicum; echinacea, unspecified; nitric acid; rancid beef; solanum dulcamara flower; 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 Liddell Laboratories, Inc. on July 07, 2011.
How is this Liddell Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845012601. 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.