Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Pollen Distress NDC 50845-0284
Onion 6 [hp_X]/mL + 13 more ingredients · Spray · Oral · Liddell Laboratories, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50845-0284-2 | 50845028402 | 1 BOTTLE, SPRAY in 1 CARTON (50845-0284-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0284-1)Marketed from Jan 26, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Pollen Distress
- Generic name (nonproprietary)
- 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
- Active ingredients
- Onion — 6 [hp_X]/mLApis mellifera — 6 [hp_X]/mLAralia racemosa root — 6 [hp_X]/mLArundo pliniana root — 30 [hp_C]/mLBaptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 4 [hp_X]/mLEuphrasia stricta — 6 [hp_X]/mLGelsemium sempervirens root — 200 [hp_C]/mLHistamine dihydrochloride — 12 [hp_X]/mLLycopodium clavatum spore — 6 [hp_X]/mLToxicodendron pubescens leaf — 200 [hp_X]/mLSchoenocaulon officinale seed — 6 [hp_C]/mLSanguinaria canadensis root — 200 [hp_C]/mLUrtica urens whole — 3 [hp_X]/mL
- Dosage form
- Spray
- Route
- Oral
- Labeler
- Liddell Laboratories, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Vegetable Proteins (Chemical structure)
- Identifiers
- Product ID 50845-0284_930a8c2f-6dcc-4179-8cc1-0724922b5d01SPL ID 930a8c2f-6dcc-4179-8cc1-0724922b5d01SPL set ID 034fcd90-81f7-4597-b58b-e2ed7047f6bdUNII 492225Q21H, 7S82P3R43Z, T90W4582DU, ZXE7LB03WC, 5EF0HWI5WU, VB06AV5US8, C9642I91WL, 639KR60Q1Q, 3POA0Q644U, C88X29Y479, 6IO182RP7A, 6NAF1689IO, N9288CD508, IHN2NQ5OF9UPC 0363113112962
- Pharmacologic class
- Non-Standardized Food Allergenic Extract; Standardized Insect Venom Allergenic Extract
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N450845028402followed by a unit qualifier and the quantityPackage 50845-0284-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS: May temporarily relieve these symptoms associated with seasonal pollen distress: • runny nose • itchy, watery eyes • rash • headache • sneezing** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.