Frankincense and Myrrh Neuropathy Aconitum Napellus, Bryonia Alba, Hypericum Perforatum 3 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL Oil — NDC 42346-0301-59 package photo

Frankincense and Myrrh Neuropathy Aconitum Napellus, Bryonia Alba, Hypericum Perforatum 3 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL Oil

by Wise Consumer Products · 1 BOTTLE, DROPPER in 1 CARTON (42346-301-59) / 59 mL in 1 BOTTLE, DROPPER
NDC 42346-0301-59
🏷️ FDA NDC (as labeled) 42346-301-59 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 42346-301-59
Product NDC 42346-301
11-digit billing NDC 42346030159
UNII U0NQ8555JD, T7J046YI2B, XK4IUX8MNB
SPL Set ID 9310c00d-c60a-4e9a-b1c1-06e6bdbb24ef
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-06-11
Route TOPICAL
Dosage form OIL
Substance ACONITUM NAPELLUS; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM
Why two NDCs? The FDA registers this code as 42346-301-59 — a 5-3-2 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 product segment → 42346-0301-59. 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

LabelerWise Consumer Products
Labeler code42346
First marketedJun 2013
Product typeHuman Otc Drug
Portfolio7 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 a topical oil containing three ingredients used in homeopathic practice: aconitum napellus, bryonia alba root, and hypericum perforatum. In homeopathic tradition, these substances are prepared according to homeopathic methods and are intended to address symptoms related to neuropathy. This product is marketed based on homeopathic principles and has not been evaluated by the FDA for effectiveness or safety. Homeopathic products are not the same as FDA-approved medicines.

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 H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII 39W1PKE3JI
    Bergamot oil is a citrus extract from bergamot orange peel. It's used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • UNII E5GY4I6YCZ
    A fragrant liquid extracted from cinnamon bark, used as a flavoring agent to improve the taste of medicines and make them more pleasant to take.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII 67ZYA5T02K
    Frankincense oil is a natural aromatic extract from tree resin. In medicines, it's used as a fragrance and flavoring agent to improve taste and smell, and may also help preserve the product.
  • UNII 5Q1I94P4WG
    A fragrant essential oil derived from geranium plants, used as a flavoring and fragrance agent to improve the taste and smell of medicines.
  • UNII I9GRO824LL
    Lemon oil is a natural fragrant extract from lemon peel. It's used in medicines as a flavoring agent to mask unpleasant tastes and improve how the medicine tastes to patients.
  • UNII H74221J5J4
    Myrrh oil is a fragrant resin extracted from myrrh tree bark. It is used in medicines as a flavoring agent and to add aroma or taste to the product.
  • UNII Z1CLM48948
    Nutmeg oil is a natural aromatic extract from nutmeg seeds. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance to mask bitter or unpleasant odors.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.

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

The official label also statesBoswellia Carterii (Frankincense) Oil, Cinnamomum Zeylanicum (Cinnamon) Leaf Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Limon (Lemon) Peel Oil, Commiphora Myrrha (Myrrh) Oil, Eucalyptus Globulus Leaf Oil, Helianthus Annuus (Sunflower) Seed Oil, Myristica Fragrans (Nutmeg) Kernel Oil, Mentha Piperita (Peppermint) Oil, Pelargonium Graveolens (Geranium) Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Tocopherol.

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 DailyMedingredient 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 eachPer 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Frankincense and Myrrh Neuropathy 3 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mLthis 42346-0301-59 Wise 1 bottle FDA listed
Frankincense and Myrrh Arthritis Pain Relief 3 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL 42346-0725-59 Wise 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

🏛️
2013
On the market since
Jun 2013
📍
2026
Currently FDA-listed
13 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
42346-0301-59 You're viewing this 1 BOTTLE, DROPPER in 1 CARTON (42346-301-59) / 59 mL in 1 BOTTLE, DROPPER 2013-06-11 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Frankincense and Myrrh Neuropathy Aconitum Napellus, Bryonia Alba, Hypericum Perforatum 3 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL OIL 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 FDA registers it as 42346-301-59, 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: 42346-0301-59, written without dashes as 42346030159. 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 42346-0301-59, the first segment (42346) is the labeler code FDA assigned to Wise Consumer Products; the middle segment (0301) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (59) 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 Wise Consumer Products. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Wise Consumer Products 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 20 words

Uses: For temporary relief of the symptoms of neuropathy such as: pain numbness tingling weakness As per Homeopathic Materia Medica

⏱️ Dosage and Administration 51 words

Directions: Adults and children 12 years of age and older: apply 10-30 drops into palm or hand and massage into feet or hands and affected areas massage oil in hand to coat painful areas can be used up to 4 times daily children under 12 years of age: consult a physician

⚠️ Warnings 141 words

Warnings: For external use only. Do not apply to wounds, broken or damaged skin apply over large areas of the body When using this product avoid contact with eyes, mouth, nose or mucous membranes do not bandage tightly Stop use and ask a doctor if you are experiencing nerve pain in the feet and hands that includes burning, shooting, prickling/tingling pains, numbness or itching as these can be signs of diabetic neuropathy. See a healthcare professional regularly if you have or suspect you have these symptoms. condition worsens if symptoms persist for more than 7 days or clear up and occur again within a few days excessive skin irritation occurs If pregnant or breastfeeding , ask a health care professional before use.

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 28 words

Other Information: store at room temperature. tamper resistant: do not use if seal around the neck of bottle is broken or missing. keep carton, it contains important information.

🧪 Active Ingredient 35 words

Active Ingredients Aconitum napellus 3X HPUS Bryonia alba 3X HPUS Hypericum perforatum 3X HPUS The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 55 words

Inactive Ingredients: Boswellia Carterii (Frankincense) Oil, Cinnamomum Zeylanicum (Cinnamon) Leaf Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Limon (Lemon) Peel Oil, Commiphora Myrrha (Myrrh) Oil, Eucalyptus Globulus Leaf Oil, Helianthus Annuus (Sunflower) Seed Oil, Myristica Fragrans (Nutmeg) Kernel Oil, Mentha Piperita (Peppermint) Oil, Pelargonium Graveolens (Geranium) Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Tocopherol.

🎯 Purpose 16 words

Purpose Aconitum napellus 3X HPUS...................Minor Pain Reliever Bryonia alba 3X HPUS............................Anti-inflammatory Hypericum perforatum 3X HPUS.............Topical Analgesic

📋 Description 75 words

Manufactured in New Hampshire for: Wise Consumer Products Co. PO Box 42400 Cincinnati, OH 45242 www.frankincensemyrrh.com Keep this carton - it contains important information Temporarily relieves the pain of NEUROPATHY Frankincense and Myrrh TM Neuropathy is specifically formulated to deliver temporary and topical relief for Neuropathy. The plant extract formula blends homeopathic ingredients in a base of sunflower oil and 10 essential oils.

Blended in an FDA registered and inspected facility in the United States.

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