NDC product

Pollen Distress

NDC 50845-0284 · Liddell Laboratories, Inc.

Key facts

Product NDC 50845-0284
Proprietary name Pollen Distress
Nonproprietary name Allium Cepa, Apis Mellifica, Aralia Racemosa, Arundo Mauritanica, Baptisia Tinctoria, Echinacea (Angustifolia), Euphrasia Officinalis, Gelsemium Sempervirens, Histaminum Hydrochloricum, Lycopodium Clavatum, Rhus Tox, Sabadilla and 2 more
Substances ONION, APIS MELLIFERA, ARALIA RACEMOSA ROOT, ARUNDO PLINIANA ROOT, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, EUPHRASIA STRICTA, GELSEMIUM SEMPERVIRENS ROOT, HISTAMINE DIHYDROCHLORIDE, LYCOPODIUM CLAVATUM SPORE, TOXICODENDRON PUBESCENS LEAF, SCHOENOCAULON OFFICINALE SEED and 2 more
Dosage form SPRAY
Route ORAL
Labeler Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
Marketing category UNAPPROVED HOMEOPATHIC
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE] and 3 more
Marketing start Jan 26, 2026
Listing certified through Dec 31, 2027

At a glance

  • 1–9 Package NDCs

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The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.

Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date:

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