Pollen-Weeds NDC 55714-2500

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2500Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2500Add 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 NDC	11-digit (billing)	Package	Copy
55714-2500-1	55714250001	28 g in 1 BOTTLE, GLASS (55714-2500-1)Marketed from Jan 1, 2019

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-Weeds
Generic name (nonproprietary): ginkgo biloba, hydrastis canadensis, taraxacum officinale, adrenalinum , aletris farinosa, alfalfa, allium cepa, antimonium tartaricum, arsenicum album, artemisia vulgaris, baptisia tinctoria, bellis perennis, berberis vulgaris, bryonia, calluna vulgaris, flos, chelidonium majus, chenopodium anthelminticum, dioscorea vilosa, euphrasia officinalis, fagus sylvatica, fraxinus americana, gelsemium sempervirens, histaminum hydrochloricum, kali bichromicum, kali iodatum, lachesis mutus, lilium tigrinum,
Active ingredients: Parthenium hysterophorus — 16 [hp_X]/gXerophyllum asphodeloides — 15 [hp_X]/gArtemisia vulgaris root — 15 [hp_X]/gEpinephrine — 15 [hp_X]/gAlfalfa — 15 [hp_X]/gAletris farinosa root — 15 [hp_X]/gBellis perennis — 15 [hp_X]/gDysphania ambrosioides — 15 [hp_X]/gLycopus virginicus — 15 [hp_X]/gPhytolacca americana root — 15 [hp_X]/gPopulus balsamifera leaf bud — 15 [hp_X]/gPopulus tremuloides leaf — 15 [hp_X]/gPtelea trifoliata bark — 15 [hp_X]/gSambucus nigra flowering top — 15 [hp_X]/gTrillium erectum root — 15 [hp_X]/gElymus repens root — 15 [hp_X]/gUrtica urens — 15 [hp_X]/gWyethia helenioides root — 15 [hp_X]/gYucca filamentosa — 16 [hp_X]/gHistamine dihydrochloride — 15 [hp_X]/gJuniperus virginiana twig — 16 [hp_X]/gThyroid, Unspecified — 15 [hp_X]/gUstilago maydis — 15 [hp_X]/gOnion — 15 [hp_X]/gAntimony potassium tartrate — 15 [hp_X]/gArsenic trioxide — 15 [hp_X]/gBaptisia tinctoria root — 15 [hp_X]/gBerberis vulgaris root bark — 15 [hp_X]/gBryonia alba root — 15 [hp_X]/gChelidonium majus — 15 [hp_X]/gEuphrasia stricta — 15 [hp_X]/gGelsemium sempervirens root — 15 [hp_X]/gPotassium dichromate — 15 [hp_X]/gPotassium iodide — 15 [hp_X]/gLachesis muta venom — 15 [hp_X]/gLycopodium clavatum spore — 15 [hp_X]/gAnemone pulsatilla — 15 [hp_X]/gSchoenocaulon officinale seed — 15 [hp_X]/gDioscorea villosa tuber — 15 [hp_X]/gGinkgo — 6 [hp_X]/gTaraxacum officinale — 6 [hp_X]/gGoldenseal — 6 [hp_X]/gQuercus robur nut — 15 [hp_X]/gCalluna vulgaris flowering top — 15 [hp_X]/gUlmus rubra bark — 16 [hp_X]/gFagus sylvatica nut — 15 [hp_X]/gTrifolium pratense flower — 15 [hp_X]/gFraxinus americana bark — 15 [hp_X]/gLilium lancifolium whole flowering — 15 [hp_X]/gRosa damascena flowering top — 15 [hp_X]/gSalix nigra bark — 15 [hp_X]/g
Dosage form: Pellet
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Fungal 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 55714-2500_2d95425f-f2e8-8194-e063-6294a90aa39fSPL ID 2d95425f-f2e8-8194-e063-6294a90aa39fSPL set ID 9caafbca-c8f7-d898-e053-2995a90a357aUNII 151F45R21P, 9I4XB1GP2B, 32MP823R8S, YKH834O4BH, DJO934BRBD, O021JGR97X, 2HU33I03UY, 4H5RSU087I, TWH5125Q6F, 11E6VI8VEG, 9CQ6C00G3C, 7IIH57D9E0, 5KQR6FTT0D, CT03BSA18U, AHW6F0T2X0, 3IXW0F6P8W, IHN2NQ5OF9, J10PD1AQ0N, T6VR38UJ9I, 3POA0Q644U, 532BCG080L, 0B4FDL9I6P, 4K7Z7K7SWG, 492225Q21H, DL6OZ476V3, S7V92P67HO, 5EF0HWI5WU, 1TH8Q20J0U, T7J046YI2B, 7E889U5RNN, C9642I91WL, 639KR60Q1Q, T4423S18FM, 1C4QK22F9J, VSW71SS07I, C88X29Y479, I76KB35JEV, 6NAF1689IO, IWY3IWX2G8, 19FUJ2C58T, 39981FM375, ZW3Z11D0JV, Q7MU1F4GLY, D9PC510CQV, 91QY4PXU8Q, I57ERU2601, 4JS0838828, 0B24UR1O1S, X67Z2963PI, 21W82Q764G, QU52J3A5B3
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N455714250001 followed by a unit qualifier and the quantity

Package 55714-2500-01. 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 Feb 7, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms of Spring and early Summer pollens such as itchy eyes, sneezing, post-nasal drip, sore throat and sinus pressure.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)