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Nail Fungus Control Calendula Officinalis Flowering Top and Silicon Dioxide 6 [hp_X]/1000mL; 6 [hp_X]/1000mL Solution/ Drops, 33 mL — NDC 51393-6988-02 package photo

Nail Fungus Control Calendula Officinalis Flowering Top and Silicon Dioxide 6 [hp_X]/1000mL; 6 [hp_X]/1000mL Solution/ Drops, 33 mL

by Forces of Nature · 33 mL in 1 BOTTLE, DISPENSING (51393-6988-2)
NDC 51393-6988-02
🏷️ FDA NDC (as labeled) 51393-6988-2 billing pads the package segment with a zero
This package
Contains33 mL Pack sizes4 compare ↓
Also comes in: 30 mL 51393-6988-03 5 ml 51393-6988-05 11 ml 51393-6988-01
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
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

FDA NDC (as labeled) 51393-6988-2
Product NDC 51393-6988
11-digit billing NDC 51393698802
UNII 18E7415PXQ, ETJ7Z6XBU4
UPC 0830743009059
SPL Set ID b7239e23-326e-4c1d-a080-55f457f1c454
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2011-04-06
Route TOPICAL
Dosage form SOLUTION/ DROPS
Substance CALENDULA OFFICINALIS FLOWERING TOP; SILICON DIOXIDE
Why two NDCs? The FDA registers this code as 51393-6988-2 — 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 → 51393-6988-02. 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 homeopathic solution marketed for nail fungus control, applied topically as drops. It contains calendula officinalis flowering top and silicon dioxide in homeopathic dilutions. In homeopathic practice, calendula is traditionally used for skin and wound care, while silicon dioxide is used in various homeopathic formulations. Homeopathic products are based on traditional use rather than clinical evidence and are not evaluated by the FDA for safety or effectiveness.

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.

💊 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.

5 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* *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 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: 30 mL 5 ml 11 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Acne/Pimple Control 6 [hp_X]/1000mL; 6 [hp_X]/1000mL 51393-6112-01 Forces 11 ml — — Discontinued —
Nail Fungus Control 6 [hp_X]/1000mL; 6 [hp_X]/1000mLthis 51393-6988-02 Forces 33 ml — — 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

🏛️
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 NDCDescription Marketing startStatus
51393-6988-01 11 mL in 1 BOTTLE, DISPENSING (51393-6988-1) 2011-04-06 Active
51393-6988-02 You're viewing this 33 mL in 1 BOTTLE, DISPENSING (51393-6988-2) 2011-04-06 Discontinued by firm
51393-6988-03 1 BOTTLE, DISPENSING in 1 CARTON (51393-6988-3) / 30 mL in 1 BOTTLE, DISPENSING 2021-06-01 Active
51393-6988-05 5 mL in 1 BOTTLE (51393-6988-5) 2016-07-01 Active

Pack size FAQ

What quantity is in NDC 51393-6988-02?
NDC 51393-6988-02 contains 33 mL — 33 ml in 1 bottle, dispensing.
What is the difference between NDC 51393-6988-02 and NDC 51393-6988-05?
Both are Nail Fungus Control Calendula Officinalis Flowering Top and Silicon Dioxide 6 [hp_X]/1000mL; 6 [hp_X]/1000mL Solution/ Drops — the drug itself is identical. NDC 51393-6988-02 is the 33 mL package, while NDC 51393-6988-05 is the 5 ml package.
What NDC number is used to bill for this package of Nail Fungus Control Calendula Officinalis Flowering Top and Silicon Dioxide 6 [hp_X]/1000mL; 6 [hp_X]/1000mL Solution/ Drops?
Bill NDC 51393-6988-02 — the 11-digit billing format is 51393698802. 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 No longer marketed (per FDA listing data)

About homeopathic listings

Nail Fungus Control Calendula Officinalis Flowering Top and Silicon Dioxide 6 [hp_X]/1000mL; 6 [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.
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 FDA registers it as 51393-6988-2, 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: 51393-6988-02, written without dashes as 51393698802. 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 51393-6988-02, the first segment (51393) is the labeler code FDA assigned to Forces of Nature; the middle segment (6988) 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 1 bottle (51393-6988-03), 5 ml (51393-6988-05), 11 ml (51393-6988-01). 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.

📄 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 20 words ▾

Indications For the relief and treatment of pain, soreness and inflammation from nail fungus.Symptoms: Discolored nails Brittle nails Distorted nails

⏱️ Dosage and Administration 33 words ▾

Directions Shake well before use. Wash and dry the affected area. Brush a thin layer onto the infected nail 3 times per day, coating the nail and adjacent skin. Repeat daily as needed.

⚠️ Warnings 85 words ▾

Warnings Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction. If pregnant or breast-feeding, ask a health professional before use.

For external use only. Som 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. Keep out of the reach of children.If accidental ingestion and adverse reaction occurse, get medicial help or contact a Poison Control Center.

🧪 Active Ingredient 48 words ▾

Active Ingredients The letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homœopathic Pharmacopœia of the United States. Equal parts of: Purpose Calendula Officinalis 6X HPUS Promotes healthy skin and healing Silicea 6X HPUS Remedy for nail ulcers, fowl smelling, crippled nails

🧪 Inactive Ingredients 16 words ▾

Also Includes Clove Oil*, Lemongrass Oil*, Rose Geranium Oil*, Sesame Oil*, Tea Tree Oil* *Certified Organic

🎯 Purpose 48 words ▾

Active Ingredients The letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homœopathic Pharmacopœia of the United States. Equal parts of: Purpose Calendula Officinalis 6X HPUS Promotes healthy skin and healing Silicea 6X HPUS Remedy for nail ulcers, fowl smelling, crippled nails

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 51393-6447-01 · Forces 51393-6989-01 · 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.