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Allergy Maximum Strength Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mL Solution/ Drops — NDC 51393-5001-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Allergy Maximum Strength Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mL Solution/ Drops — NDC 51393-5001-3 (Billing 51393-5001-03)

by Forces of Nature · 1 BOTTLE, DISPENSING in 1 CARTON / 30 mL in 1 BOTTLE, DISPENSING

This is a package of Allergy Maximum Strength Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mL Solution/ Drops from Forces of Nature, marketed since Feb 2019 and currently FDA-listed.

NDC 51393-5001-03
🏷️ FDA NDC (as labeled) 51393-5001-3 billing pads the package segment with a zero
This package
Contains30 mL in 1 bottle, dispensing Pack sizes2 compare ↓
Product page 51393-5001-01 Also comes in: 10 mL 51393-5001-1
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 51393-5001-3
Product NDC 51393-5001
11-digit billing NDC 51393500103
UNII 710FLW4U46, TRW2FUF47H, E55SMD6DA8, DTN01M69SN, 5EXL5H740Y, 451W47IQ8X +1 more
SPL Set ID 122ca23e-43f1-4e5c-afc2-1418b1717679
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-02-01
Route SUBLINGUAL
Dosage form SOLUTION/ DROPS
Substance URTICA DIOICA WHOLE; ALTHAEA OFFICINALIS ROOT; INULA HELENIUM ROOT; ANGELICA ARCHANGELICA ROOT; PINE NEEDLE OIL (PINUS SYLVESTRIS); SODIUM CHLORIDE; SILICON DIOXIDE
Why two NDCs? The FDA registers this code as 51393-5001-3 — 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 → 51393-5001-03. 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.

Clinical

🧪 What is this product?

This is an unapproved homeopathic solution delivered as sublingual drops. It contains seven ingredients, including plant materials like nettle (Urtica dioica), marshmallow root (Althaea officinalis), elecampane root (Inula helenium), and angelica root (Angelica archangelica), along with pine needle oil, sodium chloride, and silicon dioxide. In homeopathic practice, these plant ingredients are traditionally used to address allergy symptoms. Homeopathic products are not evaluated by the FDA for effectiveness and are marketed based on homeopathic tradition rather than established medical evidence.

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.

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: 10 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
51393-5001-01 51393-5001-1 Main listing 1 BOTTLE, DISPENSING in 1 CARTON / 10 mL in 1 BOTTLE, DISPENSING 2019-02-01 — Active
51393-5001-03 You're viewing this 1 BOTTLE, DISPENSING in 1 CARTON / 30 mL in 1 BOTTLE, DISPENSING 2021-10-15 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle, dispensing in 1 carton / 30 ml in 1 bottle, dispensing.
What NDC number is used to bill for this package of Allergy Maximum Strength Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mL Solution/ Drops?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Allergy Maximum Strength 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mLthis 51393-5001-03 Forces 1 bottle — — 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

🏛️
2019
On the market since
Feb 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.

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 statesDistilled Water, Grain Alcohol

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.

Manufacturer & labeler

LabelerForces of Nature
Labeler code51393
First marketedFeb 2019
Product typeHuman Otc Drug
Portfolio25 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.

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses For the temporary relief of allergy and hay fever symptoms including: Sneezing Runny Nose Itchy Eyes, Nose, Throat

⏱️ Dosage and Administration 45 words ▾

Directions Shake well before use. For best results, use at the first sign of symptoms. Place 5-10 drops under the tongue. Repeat as needed, up to every 15 minutes until symptoms improve. For ongoing immune support, use 5 - 10 drops under the tongue daily.

⚠️ Warnings 62 words ▾

Warnings For oral (sublingual) use. Ask a doctor before use in children under 3 years of age. Stop use and ask doctor if symptoms persist for more than 3 days or worsen. When using this product, rinse right away with water if it gets in the eyes. If pregnant or breast-feeding ask a doctor before use. Keep out of reach of children.

📦 Storage and Handling 17 words ▾

Other information Store in a cool, dark place Store upright Tighten cap after use to prevent oxidation

🧪 Active Ingredient 55 words ▾

Active ingredients Urtica Dioica Certified Organic 8C Treats Hives or Other Rash-Like Eruptions Althaea Officinalis 34C For Itching, Rash Like Symptoms Inula Helenium 55C Expectorant, for Respiratory Issues Angelica Archangelica 89C Remedy for Inflammation/Allergy Symptoms Pinus Sylvestris 89C Relieves Itching Natrum Muriaticum 55C Itchy Eyes/Hay Fever Relief 89C (Source of Silica) To Clear Sinus Congestion

🧪 Inactive Ingredients 6 words ▾

Inactive ingredients Distilled Water, Grain Alcohol

🎯 Purpose 55 words ▾

Active ingredients Urtica Dioica Certified Organic 8C Treats Hives or Other Rash-Like Eruptions Althaea Officinalis 34C For Itching, Rash Like Symptoms Inula Helenium 55C Expectorant, for Respiratory Issues Angelica Archangelica 89C Remedy for Inflammation/Allergy Symptoms Pinus Sylvestris 89C Relieves Itching Natrum Muriaticum 55C Itchy Eyes/Hay Fever Relief 89C (Source of Silica) To Clear Sinus Congestion

📄 Ask a Doctor Before Use If 12 words ▾

Ask a doctor before use in children under 3 years of age.

📄 Stop Use and Ask a Doctor If 30 words ▾

Stop use and ask doctor if symptoms persist for more than 3 days or worsen. When using this product, rinse right away with water if it gets in the eyes.

🤰 If Pregnant or Breast-Feeding 9 words ▾

If pregnant or breast-feeding ask a doctor before use.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 12 words ▾

Questions or comments? Call us at 1-877-975-3797 or visit our website www.forcesofnaturemedicine.com

📄 Package Label / Principal Display Panel 66 words ▾

PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton Homeopathic NDC #51393-5001-1 FORCES OF NATURE Trusted Plant Remedies Allergy Relief MAXIMUM STRENGTH FAST MULTI-SYMPTOM RELIEF with Stinging Nettle & Marsh-mallow • Calms sneezing, itching, congestion • For indoor & outdoor allergies • Non-drowsy NON-GMO Project VERIFIED nongmoproject.org USDA ORGANIC Contains 15% Alcohol 10 ml (.34 FL OZ) PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton carton image

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide — the ingredient across all brands.

Top reported reactions

Death81
Nausea28
Exposure To Toxic Agent22
Pain22
Fatigue21
Diarrhoea19
Malaise17

Age at onset

Adult4
Elderly4

Reporter sex

400 reports
Male · 32%
Female · 68%

Serious outcomes

Death109
Hospitalization54
Life-threatening4
Disabling4
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 52 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.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Allergy Maximum Strength Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide 8 [hp_C]/100mL; 34 [hp_C]/100mL; 55 [hp_C]/100mL; 89 [hp_C]/100mL; 89 [hp_C]/100mL; 55 [hp_C]/100mL SOLUTION/ DROPS 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.
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Forces of Nature. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 bottle (51393-5001-01). 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?
Forces of Nature 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.
← 51393-5000-01 · Forces 51393-5003-01 · Forces →
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.