What is NDC 55714-2562?

55714-2562 is the product NDC for Hay Fever, Lilium lancifolium whole flowering 15 [hp_X]/mL + 54 more ingredients liquid, listed with the FDA by Newton Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Hay Fever (Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Alfalfa, Allium cepa, Ambrosia artemisiaefolia, Ammonium carbonicum, Aralia racemosa, Arsenicum album, Artemisia vulgaris, Arundo mauritanica, Bellis perennis, Berberis vulgaris, Bryonia, Calluna vulgaris, flos, Chelidonium majus, Chenopodium anthelminticum, Cistus canadensis, Drosera, Dulcamara, Eupatorium perfoliatum, Euphrasia officinalis, Fagus sylvatica, Fraxinus americana, Gelsemium sempervirens).

What is the active ingredient?

Lilium lancifolium whole flowering, Sodium chloride, Populus balsamifera leaf bud, Anemone pulsatilla, Eupatorium perfoliatum flowering top, Euphrasia stricta, Gelsemium sempervirens root, Onosmodium virginianum, Schoenocaulon officinale seed, Sanguinaria canadensis root, Solidago virgaurea flowering top, Trillium erectum root, Ulmus rubra bark, Histamine dihydrochloride, Xerophyllum asphodeloides, Ustilago maydis, Parthenium hysterophorus, Potassium iodide, Lycopodium clavatum spore, Populus tremuloides leaf, Rosa x damascena flowering top, Salix nigra bark, Elymus repens root, Datura stramonium, Urtica urens, Wyethia helenioides root, Quercus robur nut, Apis mellifera, Goldenseal, Taraxacum officinale, Aconitum napellus, Alfalfa, Onion, Ambrosia artemisiifolia, Ammonium carbonate, Aralia racemosa root, Arsenic trioxide, Artemisia vulgaris root, Arundo pliniana root, Bellis perennis, Berberis vulgaris root bark, Bryonia alba root, Calluna vulgaris flowering top, Chelidonium majus, Dysphania ambrosioides, Helianthemum canadense, Drosera anglica, Solanum dulcamara top, Echinacea, Unspecified, Fagus sylvatica nut, Fraxinus americana bark, Calcium sulfide, Potassium dichromate, Lachesis muta venom, Rhododendron tomentosum leafy twig.

Newton Laboratories, Inc., NDC labeler code 55714. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hay Fever?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hay Fever NDC 55714-2562 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2562Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2562Add 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
55714-2562-1	5571425620155714256201	30 mL in 1 BOTTLE, GLASS (55714-2562-1)Marketed from May 18, 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): Hay Fever
Generic name (nonproprietary): apis mellifica, echinacea, hydrastis canadensis, taraxacum officinale, aconitum napellus, alfalfa, allium cepa, ambrosia artemisiaefolia, ammonium carbonicum, aralia racemosa, arsenicum album, artemisia vulgaris, arundo mauritanica, bellis perennis, berberis vulgaris, bryonia, calluna vulgaris, flos, chelidonium majus, chenopodium anthelminticum, cistus canadensis, drosera, dulcamara, eupatorium perfoliatum, euphrasia officinalis, fagus sylvatica, fraxinus americana, gelsemium sempervirens
Active ingredients: Lilium lancifolium whole flowering — 15 [hp_X]/mLSodium chloride — 15 [hp_X]/mLPopulus balsamifera leaf bud — 15 [hp_X]/mLAnemone pulsatilla — 15 [hp_X]/mLEupatorium perfoliatum flowering top — 15 [hp_X]/mLEuphrasia stricta — 15 [hp_X]/mLGelsemium sempervirens root — 15 [hp_X]/mLOnosmodium virginianum — 15 [hp_X]/mLSchoenocaulon officinale seed — 15 [hp_X]/mLSanguinaria canadensis root — 15 [hp_X]/mLSolidago virgaurea flowering top — 15 [hp_X]/mLTrillium erectum root — 15 [hp_X]/mLUlmus rubra bark — 16 [hp_X]/mLHistamine dihydrochloride — 15 [hp_X]/mLXerophyllum asphodeloides — 15 [hp_X]/mLUstilago maydis — 15 [hp_X]/mLParthenium hysterophorus — 16 [hp_X]/mLPotassium iodide — 15 [hp_X]/mLLycopodium clavatum spore — 15 [hp_X]/mLPopulus tremuloides leaf — 15 [hp_X]/mLRosa x damascena flowering top — 15 [hp_X]/mLSalix nigra bark — 15 [hp_X]/mLElymus repens root — 15 [hp_X]/mLDatura stramonium — 15 [hp_X]/mLUrtica urens — 15 [hp_X]/mLWyethia helenioides root — 15 [hp_X]/mLQuercus robur nut — 15 [hp_X]/mLApis mellifera — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLTaraxacum officinale — 6 [hp_X]/mLAconitum napellus — 15 [hp_X]/mLAlfalfa — 15 [hp_X]/mLOnion — 15 [hp_X]/mLAmbrosia artemisiifolia — 15 [hp_X]/mLAmmonium carbonate — 15 [hp_X]/mLAralia racemosa root — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLArtemisia vulgaris root — 15 [hp_X]/mLArundo pliniana root — 15 [hp_X]/mLBellis perennis — 15 [hp_X]/mLBerberis vulgaris root bark — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLCalluna vulgaris flowering top — 15 [hp_X]/mLChelidonium majus — 15 [hp_X]/mLDysphania ambrosioides — 15 [hp_X]/mLHelianthemum canadense — 15 [hp_X]/mLDrosera anglica — 15 [hp_X]/mLSolanum dulcamara top — 15 [hp_X]/mLEchinacea, Unspecified — 6 [hp_X]/mLFagus sylvatica nut — 15 [hp_X]/mLFraxinus americana bark — 15 [hp_X]/mLCalcium sulfide — 15 [hp_X]/mLPotassium dichromate — 15 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mLRhododendron tomentosum leafy twig — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.NDC labeler code 55714
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 18, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)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 Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 55714-2562_a603fcb4-a171-4b63-e053-2995a90a91a0SPL ID a603fcb4-a171-4b63-e053-2995a90a91a0SPL set ID a6045b91-d361-2731-e053-2a95a90a9772UNII X67Z2963PI, 451W47IQ8X, 9CQ6C00G3C, I76KB35JEV, 1W0775VX6E, C9642I91WL, 639KR60Q1Q, 604NK4250S, 6NAF1689IO, N9288CD508, 5405K23S50, AHW6F0T2X0, 91QY4PXU8Q, 3POA0Q644U, 9I4XB1GP2B, 4K7Z7K7SWG, 151F45R21P, 1C4QK22F9J, C88X29Y479, 7IIH57D9E0, 21W82Q764G, QU52J3A5B3, 3IXW0F6P8W, G6W4F0V8Z3, IHN2NQ5OF9, J10PD1AQ0N, Q7MU1F4GLY, 7S82P3R43Z, ZW3Z11D0JV, 39981FM375, U0NQ8555JD, DJO934BRBD, 492225Q21H, 9W34L2CQ9A, NJ5VT0FKLJ, T90W4582DU, S7V92P67HO, 32MP823R8S, ZXE7LB03WC, 2HU33I03UY, 1TH8Q20J0U, T7J046YI2B, D9PC510CQV, 7E889U5RNN, 4H5RSU087I, 46G3W789Q3, J61BY05EGY, KPS1B1162N, 4N9P6CC1DX, I57ERU2601, 0B24UR1O1S, 1MBW07J51Q, T4423S18FM, VSW71SS07I, 877L01IZ0P
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Osmotic Laxative; 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

N455714256201 followed by a unit qualifier and the quantity

Package 55714-2562-01. 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 May 18, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms of late Summer and Fall 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)

About NDC 55714-2562

What is NDC 55714-2562?: 55714-2562 is the product NDC for Hay Fever, Lilium lancifolium whole flowering 15 [hp_X]/mL + 54 more ingredients liquid, listed with the FDA by Newton Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hay Fever (Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Alfalfa, Allium cepa, Ambrosia artemisiaefolia, Ammonium carbonicum, Aralia racemosa, Arsenicum album, Artemisia vulgaris, Arundo mauritanica, Bellis perennis, Berberis vulgaris, Bryonia, Calluna vulgaris, flos, Chelidonium majus, Chenopodium anthelminticum, Cistus canadensis, Drosera, Dulcamara, Eupatorium perfoliatum, Euphrasia officinalis, Fagus sylvatica, Fraxinus americana, Gelsemium sempervirens).
What is the active ingredient?: Lilium lancifolium whole flowering, Sodium chloride, Populus balsamifera leaf bud, Anemone pulsatilla, Eupatorium perfoliatum flowering top, Euphrasia stricta, Gelsemium sempervirens root, Onosmodium virginianum, Schoenocaulon officinale seed, Sanguinaria canadensis root, Solidago virgaurea flowering top, Trillium erectum root, Ulmus rubra bark, Histamine dihydrochloride, Xerophyllum asphodeloides, Ustilago maydis, Parthenium hysterophorus, Potassium iodide, Lycopodium clavatum spore, Populus tremuloides leaf, Rosa x damascena flowering top, Salix nigra bark, Elymus repens root, Datura stramonium, Urtica urens, Wyethia helenioides root, Quercus robur nut, Apis mellifera, Goldenseal, Taraxacum officinale, Aconitum napellus, Alfalfa, Onion, Ambrosia artemisiifolia, Ammonium carbonate, Aralia racemosa root, Arsenic trioxide, Artemisia vulgaris root, Arundo pliniana root, Bellis perennis, Berberis vulgaris root bark, Bryonia alba root, Calluna vulgaris flowering top, Chelidonium majus, Dysphania ambrosioides, Helianthemum canadense, Drosera anglica, Solanum dulcamara top, Echinacea, Unspecified, Fagus sylvatica nut, Fraxinus americana bark, Calcium sulfide, Potassium dichromate, Lachesis muta venom, Rhododendron tomentosum leafy twig.
Who is the labeler?: Newton Laboratories, Inc., NDC labeler code 55714. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hay Fever?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.