NDC codes

FDA NDC Directory
Product NDC (as listed)50845-0270Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50845-0270Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
50845-0270-250845027002508450270021 BOTTLE, SPRAY in 1 CARTON (50845-0270-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0270-1)Marketed from Dec 7, 2020

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 — 3 [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_C]/mLSchoenocaulon officinale seed — 6 [hp_X]/mLSanguinaria canadensis root — 200 [hp_C]/mLUrtica urens whole — 3 [hp_X]/mL
Dosage form
Spray
Route
Oral
Labeler
Liddell Laboratories, Inc.NDC labeler code 50845
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Marketing end
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 50845-0270_1858a1f0-ba02-4fd0-af56-0673e0b4af17SPL ID 1858a1f0-ba02-4fd0-af56-0673e0b4af17SPL set ID a05f7d34-9f5c-42a4-a9f5-8e62e1e86020UNII 492225Q21H, 7S82P3R43Z, T90W4582DU, ZXE7LB03WC, 5EF0HWI5WU, VB06AV5US8, C9642I91WL, 639KR60Q1Q, 3POA0Q644U, C88X29Y479, 6IO182RP7A, 6NAF1689IO, N9288CD508, IHN2NQ5OF9
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

N450845027002 followed by a unit qualifier and the quantity

Package 50845-0270-02. 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 allergies and hay fever: • 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.

Full label on DailyMed (opens in a new tab)

About NDC 50845-0270

What is NDC 50845-0270?
50845-0270 is the product NDC for Pollen Distress, Onion 6 [hp_X]/mL + 13 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
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).
What is the active ingredient?
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, Sanguinaria canadensis root, Urtica urens whole.
Who is the labeler?
Liddell Laboratories, Inc., NDC labeler code 50845. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pollen Distress?
1 other product NDC are listed under this name. See all Pollen Distress NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Pollen Distress NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Pollen Distressallium 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 urensOnion 6 [hp_X]/mL + 13 more ingredientsSprayOralLiddell Laboratories, Inc.50845-028450845-0284-02

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