Pollen Distress Spray
NDC Package 50845-0284-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Pollen Distress (allium cepa, apis mellifica, aralia racemosa, arundo mauritanica, baptisia tinctoria, echinacea (angustifolia), euphrasia officinalis, gelsemium sempervirens, histaminum hydrochloricum, lycopodium clavatum, rhus tox, sabadilla, sanguinaria canadensis, urtica urens) sprays is adults and children over 12: Spray twice under the tongue three times per day. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0284.

Identification & Billing

NDC Package Code
50845-0284-2
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0284-1)
Product Code
50845-0284
11-Digit Billing Format
50845028402

Clinical Specifications

Proprietary Name
Pollen Distress
Non-Proprietary Name
Allium Cepa, Apis Mellifica, Aralia Racemosa, Arundo Mauritanica, Baptisia Tinctoria, Echinacea (angustifolia), Euphrasia Officinalis, Gelsemium Sempervirens, Histaminum Hydrochloricum, Lycopodium Clavatum, Rhus Tox, Sabadilla, Sanguinaria Canadensis, Urtica Urens
Substance Name
Apis Mellifera; Aralia Racemosa Root; Arundo Pliniana Root; Baptisia Tinctoria Root; Echinacea Angustifolia Whole; Euphrasia Stricta; Gelsemium Sempervirens Root; Histamine Dihydrochloride; Lycopodium Clavatum Spore; Onion; Sanguinaria Canadensis Root; Schoenocaulon Officinale Seed; Toxicodendron Pubescens Leaf; Urtica Urens Whole
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Adults and children over 12: Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day.Children 12 and under: Consult a doctor prior to use.

Regulatory & Marketing

Labeler Name
Liddell Laboratories, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-26-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 50845-0284-2 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0284-1) of Pollen Distress, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains apis mellifera; aralia racemosa root; arundo pliniana root; baptisia tinctoria root; echinacea angustifolia whole; euphrasia stricta; gelsemium sempervirens root; histamine dihydrochloride; lycopodium clavatum spore; onion; sanguinaria canadensis root; schoenocaulon officinale seed; toxicodendron pubescens leaf; urtica urens whole 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 January 26, 2026. The current certification is valid through December 31, 2027.

How is this Liddell Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845028402. 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:

10-Digit Format (5-4-1)
50845-0284-2
11-Digit CMS (5-4-2)
50845-0284-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.