![Nail Fungus Control Extra Strength Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mL Solution/ Drops, 33 mL — NDC 51393-6989-02 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=d02b88a6-1999-4dcd-91b5-fad88a664fcb&name=Nail+Fungus+Control+Extra+11ml+Carton.jpg)
Nail Fungus Control Extra Strength Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mL Solution/ Drops, 33 mL
by Forces of Nature · 33 mL in 1 BOTTLE, DISPENSING (51393-6989-2)
NDC 51393-6989-02
🏷️ FDA NDC (as labeled)
51393-6989-2
billing pads the package segment with a zero
This package
Contains33 mL
Pack sizes3 compare ↓
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)
51393-6989-2
Product NDC
51393-6989
11-digit billing NDC
51393698902
UNII
18E7415PXQ, ETJ7Z6XBU4, XK4IUX8MNB
SPL Set ID
d02b88a6-1999-4dcd-91b5-fad88a664fcb
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2011-04-06
Route
TOPICAL
Dosage form
SOLUTION/ DROPS
Substance
CALENDULA OFFICINALIS FLOWERING TOP; SILICON DIOXIDE; HYPERICUM PERFORATUM WHOLE
Why two NDCs?
The FDA registers this code as 51393-6989-2 — 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 → 51393-6989-02. 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
LabelerForces of Nature
Labeler code51393
First marketedApr 2011
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.
🩺 Clinical
🧪 What is this product?
This is a topical homeopathic solution marketed for nail fungus concerns. It contains calendula officinalis flowering top, hypericum perforatum whole, and silicon dioxide in homeopathic dilutions. In homeopathic practice, calendula and hypericum are traditionally used for skin and wound-related conditions, while silicon dioxide is included as a component. Homeopathic products are marketed based on traditional use and are not evaluated by the FDA for effectiveness or safety.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
yellow
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 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 578389D6D0
Clove oil is an essential oil derived from clove plant buds. It's used in medicines as a flavoring agent and for its mild preservative properties to help maintain product stability.
-
UNII UP0M8M3VZW
A fragrant essential oil extracted from lemongrass plants, used primarily as a flavoring and fragrance agent to improve taste and aroma in oral medications.
-
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 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.
-
UNII VIF565UC2G
Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
-
UNII 2UK410MY6B
Thyme oil is an essential oil extracted from the thyme plant. It's used in medicines as a flavoring agent and preservative to improve taste and help maintain product stability.
6 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesClove Oil*, Lemongrass Oil*, Rose Geranium Oil*, Sesame Oil*, Tea Tree Oil*, Thyme Oil* *Certified Organic
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
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 |
|---|---|---|---|---|---|---|
| Nail Fungus Control Extra Strength 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mLthis 51393-6989-02 | Forces | 33 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
🏛️
2011
On the market since
Apr 2011
📍
2026
Currently FDA-listed
15 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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 51393-6989-01 | 11 mL in 1 BOTTLE, DISPENSING (51393-6989-1) | 2011-04-06 | Active |
| 51393-6989-02 You're viewing this | 33 mL in 1 BOTTLE, DISPENSING (51393-6989-2) | 2011-04-06 | Active |
| 51393-6989-03 | 30 mL in 1 BOTTLE, DISPENSING (51393-6989-3) | 2021-06-01 | Active |
You're viewing the largest of 3 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 51393-6989-02?
NDC 51393-6989-02 contains 33 mL — 33 ml in 1 bottle, dispensing.
What is the difference between NDC 51393-6989-02 and NDC 51393-6989-01?
Both are Nail Fungus Control Extra Strength Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mL Solution/ Drops — the drug itself is identical. NDC 51393-6989-02 is the 33 mL package, while NDC 51393-6989-01 is the 11 ml package.
What NDC number is used to bill for this package of Nail Fungus Control Extra Strength Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mL Solution/ Drops?
Bill NDC 51393-6989-02 — the 11-digit billing format is 51393698902. 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
About homeopathic listings
Nail Fungus Control Extra Strength Calendula Officinalis Flowering Top, Silicon Dioxide, and Hypericum Perforatum 8 [hp_X]/1000mL; 8 [hp_X]/1000mL; 8 [hp_X]/1000mL 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 FDA registers it as 51393-6989-2, 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: 51393-6989-02, written without dashes as 51393698902. 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 51393-6989-02, the first segment (51393) is the labeler code FDA assigned to Forces of Nature; the middle segment (6989) 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.
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 2 other package presentations of this same product, including 11 ml (51393-6989-01), 30 ml (51393-6989-03). 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.
📄 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 ▾
Uses for the relief and treatment of pain, soreness and inflammation from nail fungus. Symptoms: Discolored nails, Brittle nails, Distorted nails
⏱️ Dosage and Administration ▾
Directions Shake well before use. Wash and dry the affected area. Brush a thin layer onto the affected nail 3 times per day, coating the nail and adjacent skin. Repeat daily as needed.
⚠️ Warnings ▾
Warnings Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2without physician direction. Keep out of the reach of children.
If accidental ingestion and adverse reacton occurs, get medical help or contact a Poison Control Center. For External Use Only. Some individuals may be sensitive to essential oils.
Begin with a small drop to determine if product causes any irritation. Pregnancy and Breastfeeding If pregnant or breastfeeding, ask a health professional before use.
Pregnancy and Breastfeeding If pregnant or breastfeeding, ask a health professional before use.
🧪 Active Ingredient ▾
Active Ingredients Purpose Calendula Officinalis* 8X Promotes Healthy Skin and Healing Hypericum Perforatum* 8X Remedies for Difficulties with Nails Equisetum Arvense* 8X (Source of Silica) Remedy for Foul Smelling Nail Ulcerts *Certified Organic
🧪 Inactive Ingredients ▾
Inactive Ingredients Clove Oil*, Lemongrass Oil*, Rose Geranium Oil*, Sesame Oil*, Tea Tree Oil*, Thyme Oil* *Certified Organic
🎯 Purpose ▾
Active Ingredients Purpose Calendula Officinalis* 8X Promotes Healthy Skin and Healing Hypericum Perforatum* 8X Remedies for Difficulties with Nails Equisetum Arvense* 8X (Source of Silica) Remedy for Foul Smelling Nail Ulcerts *Certified Organic
No label section mentions that — try another word, or open the full label on DailyMed below.
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.