NDC 55714-4855-01 — Allergies Apis mellifica, Echinacea

🆔 Identity & classification

FDA NDC (as labeled) 55714-4855-1

Product NDC 55714-4855

11-digit billing NDC 55714485501

UNII 91QY4PXU8Q, 24HBF856C8, 6NAF1689IO, CT03BSA18U, N9288CD508, TWH5125Q6F +12 more

SPL Set ID 0631d5e5-9da4-bcb7-e063-6394a90a62de

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 On market

FDA listing status Listed (active directory)

Marketing start 2023-09-25

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 55714-4855-1 — 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 → 55714-4855-01. 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 marketedSep 2023

Product typeHuman Otc Drug

Portfolio270 products on file

🔎 All NDCs from Newton Laboratories, Inc.

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 product taken by mouth that contains numerous plant, insect, and mineral ingredients traditionally used in homeopathic practice for allergy-related symptoms. The formula includes botanical extracts such as echinacea, hydrastis, and alfalfa, along with bee venom and various other plant and mineral substances. Homeopathic products are marketed based on homeopathic tradition rather than evaluated by the FDA for effectiveness or safety. This product is not approved as a conventional drug.

Patient education

📘 MedlinePlus patient leaflet ↗

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 system	Per mL	Per 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.

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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Allergies 21 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [this 55714-4855-01	Newton	30 ml	—	—	FDA listed	—

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

🏛️

2023

On the market since

Sep 2023

📍

2026

Currently FDA-listed

3 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

Serious outcomes

Hospitalization2

Reports over time (by year) — tap or hover for the count & year

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 NDC	Description	Marketing start	Status
55714-4855-01 You're viewing this	30 mL in 1 BOTTLE, GLASS (55714-4855-1)	2023-09-25	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

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 21 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [hp_X]/mL; 20 [ 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	— Not published for this NDC No photo available yet for this listing.
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.

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 55714-4855-1, 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: 55714-4855-01, written without dashes as 55714485501. 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 55714-4855-01, the first segment (55714) is the labeler code FDA assigned to Newton Laboratories, Inc.; the middle segment (4855) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.

Is this package still being marketed?

Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Newton Laboratories, Inc.. Listing status can change — the directory data on this page refreshes weekly.

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 41 words ▾

DOSAGE & ADMINISTRATION SECTION Directions: Ages 12 and up take 6 drops by mouth (ages 0 to 11, give 3 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 mel 11x, Echinacea 11x, Hydrastis 11x, Taraxacum 11x, Aconitum nap 20x, Aethusa cynapium 20x, Agaricus musc 20x, Aletris 20x, Alfalfa 20x, Allium cepa 20x, Allium sat 20x, Ambrosia 20x, Arsenicum alb 20x, Artemisia 20x, Arundo ma 20x, Avena 20x, Belladonna 20x, Bellis 20x, Bovista 20x, Bromium 20x, Bryonia 20x, Caffeinum 20x, Calc carb 20x, Calluna vulgaris, flos 20x, Capsicum 20x, Cat hair 20x, Chamomilla 20x, Chelidonium maj 20x, Chenopodium anth 20x, Cinnamomum 20x, Cistus canadensis 20x, Coccus 20x, Cynara 20x, Dog hair 20x, Drosera 20x, Dulcamara 20x, Euphrasia 20x, Fagopyrum 20x, Fagus syl 20x, Fragaria 20x, Frax amer 20x, Gelsemium 20x, Histaminum hydro 20x, House dust 20x, Hyoscyamus 20x, Jequirity 20x, Juglans reg 20x, Kali iod 20x, Lac vac 20x, Ledum 20x, Lilium 20x, Lycopodium 20x, Lycopus 20x, Mentha pip 20x, Nat mur 20x, Nux mosch 20x, Onosmodium virginianum 20x, Ova tosta 20x, Phytolacca 20x, Populus can 20x, Populus trem 20x, Ptelea 20x, Pulsatilla 20x, Quercus gland sp 20x, Rhus tox 20x, Rosa dam 20x, Sabadilla 20x, Saccharinum 20x, Sac lac 20x, Salix nig 20x, Sambucus nig 20x, Sanguinaria 20x, Secale 20x, Stramonium 20x, Sulphur 20x, Tabacum 20x, Thiosinaminum 20x, Trillium 20x, Triticum 20x, Urtica ur 20x, Ustilago maidis 20x, Wyethia 20x, Xerophyllum 20x, Zingiber 20x, Anacardium occ 21x, Ascorbic ac 21x, Astacus 21x, Glycyrrhiza 21x, Juniperus virg 21x, Lycopersicum 21x, Nat nitricum 21x, Parthenium 21x, Saccharum off 21x, Sinapis nig 21x, Solanum nig 21x, Solanum tub 21x, Stigmata 21x, Torula cerevisiae 21x, Ulmus fulv 21x, Yucca 21x.

🧪 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 ↗

🔗 Related NDC lookups

🧪 All 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 NDCsSame ingredient 🏭 All Newton labeler NDCsLabeler code 55714