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Back Pain Pain Management Arnica Montana, HORSE CHESTNUT, Hypericum Perforatum, RUTA GRAVEOLENS WHOLE, and SODIUM CHLORIDE 30 [hp_C]/100mL; 6 [hp_C]/100mL; 12 [hp_C]/100mL; 30 [hp_C]/100mL; 30 [hp_C]/100mL Solution/ Drops — NDC 51393-4015-1 (Billing 51393-4015-01)

by Forces of Nature · 1 BOTTLE, DISPENSING in 1 CARTON / 11 mL in 1 BOTTLE, DISPENSING

This is a package of Back Pain Pain Management Arnica Montana, HORSE CHESTNUT, Hypericum Perforatum, RUTA GRAVEOLENS WHOLE, and SODIUM CHLORIDE 30 [hp_C]/100mL; 6 [hp_C]/100mL; 12 [hp_C]/100mL; 30 [hp_C]/100mL; 30 [hp_C]/100mL Solution/ Drops from Forces of Nature, no longer marketed (first marketed Nov 2019), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 51393-4015-01
🏷️ FDA NDC (as labeled) 51393-4015-1 billing pads the package segment with a zero
This package
Contains11 mL in 1 bottle, dispensing Pack sizes2 compare ↓
Main listing for product 51393-4015 · Also comes in: 4 mL 51393-4015-4
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

NDC database record

One package, one record: these facts belong to NDC 51393-4015-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
51393 labeler · 4015 product · 1 package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0830743013049
FDA record last changed
Jul 24, 2026
⚠️
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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 51393-4015-1
Product NDC 51393-4015
11-digit billing NDC 51393401501
UNII O80TY208ZW, 3C18L6RJAZ, XK4IUX8MNB, 181JI0338P, 451W47IQ8X
UPC 0830743013049
SPL Set ID bf089347-f334-4d6d-ab58-cf7f0b16810f
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2019-11-01
Route TOPICAL
Dosage form SOLUTION/ DROPS
Substance ARNICA MONTANA WHOLE; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; RUTA GRAVEOLENS WHOLE; SODIUM CHLORIDE
Why two NDCs? The FDA registers this code as 51393-4015-1 — 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 → 51393-4015-01. 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.

Clinical

🧪 What is this product?

This is a homeopathic liquid preparation applied to the skin for back pain management. It contains arnica montana, horse chestnut, hypericum perforatum, ruta graveolens, and sodium chloride in homeopathic potencies. In homeopathic practice, these plant-derived ingredients are traditionally used for musculoskeletal discomfort and bruising. Homeopathic products are marketed based on traditional use rather than FDA effectiveness evaluation.

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: 4 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
51393-4015-01 You're viewing this Main listing 1 BOTTLE, DISPENSING in 1 CARTON / 11 mL in 1 BOTTLE, DISPENSING 2019-11-01 — Discontinued by firm
51393-4015-04 51393-4015-4 1 BOTTLE, DISPENSING in 1 CARTON / 4 mL in 1 BOTTLE, DISPENSING 2019-11-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle, dispensing in 1 carton / 11 ml in 1 bottle, dispensing.
What NDC number is used to bill for this package of Back Pain Pain Management Arnica Montana, HORSE CHESTNUT, Hypericum Perforatum, RUTA GRAVEOLENS WHOLE, and SODIUM CHLORIDE 30 [hp_C]/100mL; 6 [hp_C]/100mL; 12 [hp_C]/100mL; 30 [hp_C]/100mL; 30 [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
Back Pain Pain Management 30 [hp_C]/100mL; 6 [hp_C]/100mL; 12 [hp_C]/100mL; 30 [hp_C]/100mL; 30 [hp_C]/100mLthis 51393-4015-01 Forces 1 bottle — — 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
Nov 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 60F80Z61A9
    A fragrant plant oil extracted from chamomile flowers. It's used as a flavoring agent and fragrance in medicines to improve taste and smell, making the product more pleasant to take.
  • UNII 9RES347CKG
    A fragrant oil derived from lavandin plants, used as a flavoring and aromatic agent to improve the taste and smell of medicines.
  • UNII 5EXL5H740Y
    A natural oil extracted from Scotch pine needles, used as a flavoring agent and fragrance component in medicines. It adds taste and aroma to improve how the medication tastes or smells.
  • UNII QX10HYY4QV
    Sesame oil is a plant-derived oil from sesame seeds. It's used in medicines as a solvent or carrier to dissolve or suspend active ingredients, helping them mix evenly throughout the formulation.

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

The official label also statesSesame Oil, Lavandin Oil, Pine Oil, German Chamomile Oil

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 marketedNov 2019
Product typeHuman Otc Drug
Portfolio25 products on file

More NDCs from Forces of Nature labeler code 51393

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 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses relieves back pain and soreness due to overuse, strain, spasm, or trauma.

⏱️ Dosage and Administration 19 words ▾

Directions shake well before use. Simply roll on the problem area. Gently rub into the skin. Apply as needed.

⚠️ Warnings 85 words ▾

Warnings For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if product causes any irritation.

Discontinue use if any irritation occurs. Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction.

Keep out of reach of children. If pregnant or breast-feeding, ask a health professional before use. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

📦 Storage and Handling 16 words ▾

Other information Keep in cool dark place store upright tighten cap after use to prevent oxidation

🧪 Active Ingredient 45 words ▾

Active ingredients Purpose Arnica montana USDA Certified Organic 30C Relief for Muscle/Tendon Pain Aesculus hippocastanum 6C Relief for Constant Backache Hypericum perforatum 12C Relief for Back/Spinal Pain Ruta graveolens 30C Relief for Pain in the Nape and Loins Natrum muriaticum 30C Relief for Lower Backache

🧪 Inactive Ingredients 14 words ▾

Inactive ingredients Sesame Oil , Lavandin Oil , Pine Oil , German Chamomile Oil

🎯 Purpose 45 words ▾

Active ingredients Purpose Arnica montana USDA Certified Organic 30C Relief for Muscle/Tendon Pain Aesculus hippocastanum 6C Relief for Constant Backache Hypericum perforatum 12C Relief for Back/Spinal Pain Ruta graveolens 30C Relief for Pain in the Nape and Loins Natrum muriaticum 30C Relief for Lower Backache

🤰 If Pregnant or Breast-Feeding 26 words ▾

If pregnant or breast-feeding, ask a health professional before use. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

📄 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 63 words ▾

PRINCIPAL DISPLAY PANEL - 11 ml Bottle Carton Homeopathic NDC #51393-4015-1 FORCES OF NATURE Back Pain ORGANIC MEDICINE Topical Pain Relief Lower Back, Neck & Shoulders Relieves Constant & Chronic Pain Natural, Long Lasting & Non Addictive Medicated Deep Penetrating Action Arnica Montana USDA ORGANIC NON GMO Project VERIFIED nongmoproject.org 11 ml (.37 FL OZ) PRINCIPAL DISPLAY PANEL - 11 ml Bottle Carton

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

About this NDC listing & data coverage

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

About homeopathic listings

Back Pain Pain Management Arnica Montana, HORSE CHESTNUT, Hypericum Perforatum, RUTA GRAVEOLENS WHOLE, and SODIUM CHLORIDE 30 [hp_C]/100mL; 6 [hp_C]/100mL; 12 [hp_C]/100mL; 30 [hp_C]/100mL; 30 [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 — 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.
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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 bottle (51393-4015-04). 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.
← 51386-0291-02 · Napoleon 51393-4016-04 · 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.