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Allergies Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Aethusa cynapium, Agaricus muscarius, Aletris farinosa, Alfalfa, Allium cepa, Allium sativum, Ambrosia artemisiaefolia, Arsenicum album, Artemisia vulgaris, Arundo m 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ Liquid, 50 mL — NDC 55714-1519-02 package photo

Allergies Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Aethusa cynapium, Agaricus muscarius, Aletris farinosa, Alfalfa, Allium cepa, Allium sativum, Ambrosia artemisiaefolia, Arsenicum album, Artemisia vulgaris, Arundo m 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ Liquid, 50 mL

by Newton Laboratories, Inc. · 50 mL in 1 BOTTLE, GLASS (55714-1519-2)
NDC 55714-1519-02
🏷️ FDA NDC (as labeled) 55714-1519-2 billing pads the package segment with a zero
This package
Contains50 mL Pack sizes2 compare ↓
Also comes in: 30 ml 55714-1519-01
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 55714-1519-2
Product NDC 55714-1519
11-digit billing NDC 55714151902
UNII 91QY4PXU8Q, 24HBF856C8, 6NAF1689IO, CT03BSA18U, N9288CD508, TWH5125Q6F +12 more
SPL Set ID 9d4c4d88-43da-49dd-e053-2995a90af18d
Established class (EPC) Vitamin C; Non-Standardized Plant Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Standardized Insect Venom Allergenic Extract; Non-Standardized Food Allergenic Extract; Central Nervous System Stimulant; Methylxanthine; Standardized Animal Hair Allergenic Extract; Non-Standardized Animal Hair Allergenic Extract; Non-Standardized House Dust Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production; Central Nervous System Stimulation
Chemical class Ascorbic Acid; Allergens; Plant Proteins; Fungal Proteins; Bee Venoms; Dietary Proteins; Vegetable Proteins; Xanthines; Dander; Salivary Proteins and Peptides; Food Additives; Animal Fur; House Dust; Milk Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2019-01-01
Route ORAL
Dosage form LIQUID
Substance ULMUS RUBRA BARK; EGG SHELL, COOKED; SCHOENOCAULON OFFICINALE SEED; SAMBUCUS NIGRA FLOWERING TOP; SANGUINARIA CANADENSIS ROOT; LYCOPUS VIRGINICUS; LACTOSE, UNSPECIFIED FORM; CLAVICEPS PURPUREA SCLEROTIUM; TRILLIUM ERECTUM ROOT; ASCORBIC ACID; BLACK MUSTAR
Why two NDCs? The FDA registers this code as 55714-1519-2 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 55714-1519-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerNewton Laboratories, Inc.
Labeler code55714
First marketedJan 2019
Product typeHuman Otc Drug
Portfolio270 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an unapproved homeopathic liquid taken by mouth that contains multiple plant, insect, and mineral ingredients traditionally used in homeopathic practice for allergy-related symptoms. The product includes substances such as apis mellifica (honeybee), various plant extracts like echinacea and allium cepa (onion), and mineral preparations like arsenicum album. Homeopathic products are marketed based on traditional homeopathic use and are not evaluated by the FDA for safety or effectiveness. Each ingredient is diluted to homeopathic potency levels in this formulation.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

2 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 30 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Allergies 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ 55714-2584-01 Newton 30 ml — — FDA listed —
Allergies 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [this 55714-1519-02 Newton 50 ml — — Discontinued —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2019
On the market since
Jan 2019
📍
2026
Currently FDA-listed
7 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Allergies (this brand).

Top reported reactions

Alanine Aminotransferase Increased1
Anxiety1
Aspartate Aminotransferase Increased1
Atrial Fibrillation1
Cough1
Covid-191
Death1

Reporter sex

7 reports

Serious outcomes

Hospitalization2
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 3 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
55714-1519-02 You're viewing this 50 mL in 1 BOTTLE, GLASS (55714-1519-2) 2019-01-01 Discontinued by firm
55714-1519-01 30 mL in 1 BOTTLE, GLASS (55714-1519-1) 2023-08-01 Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 55714-1519-02?
NDC 55714-1519-02 contains 50 mL — 50 ml in 1 bottle, glass.
What is the difference between NDC 55714-1519-02 and NDC 55714-1519-01?
Both are Allergies Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Aethusa cynapium, Agaricus muscarius, Aletris farinosa, Alfalfa, Allium cepa, Allium sativum, Ambrosia artemisiaefolia, Arsenicum album, Artemisia vulgaris, Arundo m 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ Liquid — the drug itself is identical. NDC 55714-1519-02 is the 50 mL package, while NDC 55714-1519-01 is the 30 ml package.
What NDC number is used to bill for this package of Allergies Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Aethusa cynapium, Agaricus muscarius, Aletris farinosa, Alfalfa, Allium cepa, Allium sativum, Ambrosia artemisiaefolia, Arsenicum album, Artemisia vulgaris, Arundo m 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ Liquid?
Bill NDC 55714-1519-02 — the 11-digit billing format is 55714151902. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing No longer marketed (per FDA listing data)

About homeopathic listings

Allergies Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Aethusa cynapium, Agaricus muscarius, Aletris farinosa, Alfalfa, Allium cepa, Allium sativum, Ambrosia artemisiaefolia, Arsenicum album, Artemisia vulgaris, Arundo m 16 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [hp_X]/mL; 15 [ LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 55714-1519-2, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 55714-1519-02, written without dashes as 55714151902. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 55714-1519-02, the first segment (55714) is the labeler code FDA assigned to Newton Laboratories, Inc.; the middle segment (1519) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 30 ml (55714-1519-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Newton Laboratories, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 25 words ▾

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

⏱️ Dosage and Administration 42 words ▾

DOSAGE & ADMINISTRATION SECTION Directions: Children, ages 0 to 11, give 3 drops by mouth (ages 12 and up take 6 drops) as needed or directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

⚠️ Warnings 43 words ▾

WARNINGS SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

🧪 Active Ingredient ~1 min read ▾

OTC - ACTIVE INGREDIENT SECTION Equal parts of Apis mellifica 6x, Echinacea 6x, Hydrastis canadensis 6x, Taraxacum officinale 6x, Aconitum napellus 15x, Aethusa cynapium 15x, Agaricus muscarius 15x, Aletris farinosa 15x, Alfalfa 15x, Allium cepa 15x, Allium sativum 15x, Ambrosia artemisiaefolia 15x, Arsenicum album 15x, Artemisia vulgaris 15x, Arundo mauritanica 15x, Avena sativa 15x, Belladonna 15x, Bellis perrenis 15x, Bovista 15x, Bromium 15x, Bryonia 15x, Caffeinum 15x, Calcarea carbonica 15x, Calluna vulgaris, flos 15x, Capsicum annuum 15x, Cat hair 15x, Chamomilla 15x, Chelidonium majus 15x, Chenopodium anthelminticum 15x, Cinnamomum 15x, Cistus canadensis 15x, Coccus cacti 15x, Cynara scolymus 15x, Dog hair 15x, Drosera 15x, Dulcamara 15x, Euphrasia officinalis 15x, Fagopyrum esculentum 15x, Fagus sylvatica 15x, Fragaria vesca 15x, Fraxinis americana 15x, Gelsemium sempervirens 15x, Histaminum hydrochloricum 15x, House dust 15x, Hyoscyamus niger 15x, Jequirity 15x, Juglans regia 15x, Kali iodatum 15x, Lac vaccinum 15x, Ledum palustre 15x, Lilium tigrinum 15x, Lycopodium clavatum 15x, Lycopus virginicus 15x, Mentha piperita 15x, Natrum muriaticum 15x, Nux moschata 15x, Onosmodium virginianum 15x, Ova tosta 15x, Phytolacca decandra 15x, Populus candicans 15x, Populus tremuloides 15x, Ptelea trifoliata 15x, Pulsatilla 15x, Quercus glandium spiritus 15x, Rhus toxicodendron 15x, Rosa damascena 15x, Sabadilla 15x, Saccharinum 15x, Saccharum lactis 15x, Salix nigra 15x, Sambucus nigra 15x, Sanguinaria canadensis 15x, Secale cornutum 15x, Stramonium 15x, Sulphur 15x, Tabacum 15x, Thiosinaminum 15x, Trillium pendulum 15x, Triticum repens 15x, Urtica urens 15x, Ustilago maidis 15x, Wyethia helenoides 15x, Xerophyllum asphodeloides 15x, Zingiber officinale 15x, Anacardium occidentale 16x, Ascorbicum acidum 16x, Astacus fluviatilis 16x, Glycyrrhiza glabra 16x, Juniperus virginiana 16x, Lycopersicum esculentum 16x, Natrum nitricum 16x, Parthenium 16x, Saccharum officinale 16x, Sinapis nigra 16x, Solanum nigrum 16x, Solanum tuberosum 16x, Stigmata maidis 16x, Torula cerevisiae 16x, Ulmus fulva 16x, Yucca filamentosa 16x.

🧪 Inactive Ingredients 15 words ▾

INACTIVE INGREDIENT SECTION Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

🎯 Purpose 25 words ▾

OTC - PURPOSE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 55711-0101-08 · Lofthouse 55714-1521-01 · Newton →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.