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HerpaOne GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g Ointment, 44 g — NDC 24909-0061-44 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

HerpaOne GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g Ointment, 44 g — NDC 24909-061-44 (Billing 24909-0061-44)

by Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions · 44 g in 1 JAR

This is a package of 44 g of HerpaOne GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g Ointment from Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions, marketed since Sep 2023 and currently FDA-listed, this package's marketing is listed to end Jan 2027. It is this product's only package size.

NDC 24909-0061-44
🏷️ FDA NDC (as labeled) 24909-061-44 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ 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 24909-061-44 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
24909 labeler · 061 product · 44 package
Package marketed since
Sep 26, 2023
Package marketing ended
Jan 8, 2027
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 2490906144 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 24909-061-44
Product NDC 24909-061
11-digit billing NDC 24909006144
UNII 4QQN74LH4O, 451W47IQ8X, H8FJJ6KX5Y, 1NT28V9397
SPL Set ID 6b196d97-6446-4651-97ef-6615cf3e3173
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-09-26
Marketing end 2027-01-08
Route TOPICAL
Dosage form OINTMENT
Substance GRAPHITE; SODIUM CHLORIDE; SYMPHYTUM OFFICINALE WHOLE; THUJA OCCIDENTALIS LEAFY TWIG
Why two NDCs? The FDA registers this code as 24909-061-44 — 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 → 24909-0061-44. 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?

HerpaOne Graphite is a homeopathic topical ointment containing graphite, sodium chloride, symphytum officinale (comfrey), and thuja occidentalis (arborvitae). In homeopathic practice, these ingredients are traditionally used for skin conditions, though homeopathic products are marketed based on homeopathic tradition rather than clinical evidence evaluated by the FDA. This product is not approved by the FDA for 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.

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 gPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
24909-0061-44 You're viewing this Main listing 44 g in 1 JAR 2023-09-26 Jan 8, 2027 Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
terrasil Eczema and Psoriasis Severe Outbreak 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g 24909-0060-28 Aidance 28 g — — FDA listed —
terragen HG Formula Maximum Strength 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g 24909-0062-14 Aidance 14 g — — FDA listed —
HerpaOne 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/gthis 24909-0061-44 Aidance 44 g — — 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

🏛️
2023
On the market since
Sep 2023
📍
2026
Currently FDA-listed
3 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 Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII H3E878020N
    Cottonseed oil is a natural vegetable oil extracted from cotton plant seeds. It is used in medicines as a solvent and lubricant to help dissolve active ingredients and allow smooth tablet or capsule movement through manufacturing equipment.
  • 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 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII K3Z4F929H6
    Lysine is an amino acid that serves as a buffer and pH regulator in medications. It helps maintain the medicine's stability and proper acidity level during storage and use.
  • UNII 3A3U0GI71G
    Magnesium oxide is a mineral compound that acts as a buffer and filler in medications. It helps neutralize stomach acid and adds bulk to the tablet or capsule formulation.
  • UNII 5QUO05548Z
    Palm oil is a natural plant-based fat extracted from palm fruit. It's used as a lubricant, binder, or coating agent to help the medicine hold together, flow smoothly during manufacturing, and sometimes improve how the body absorbs the active ingredient.
  • 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 4H6PCL92ZN
    Silver stearate is a metallic salt made from silver and stearic acid, a fatty substance. It works as a lubricant and glidant in tablet formulations, helping the medicine powder flow smoothly during manufacturing and preventing sticking.
  • UNII 5BIA40E9ED
    A natural essential oil extracted from lemongrass plants, used as a flavoring and fragrance agent to improve the taste and smell of the medicine.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesbeeswax, coconut oil (organic), cottonseed oil, eucalyptus oil, jojoba oil, lemongrass oil, lysine, magnesium oxide, MCT oil, peppermint oil, silver stearate, zinc oxide

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

LabelerAidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Labeler code24909
First marketedSep 2023
Product typeHuman Otc Drug
Portfolio15 products on file

More NDCs from Aidance Scientific, Inc, DBA Aidance Skincare &... labeler code 24909

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 🧪 Active Ingredient 🧪 Inactive Ingredients 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

Uses For temporary relief of swelling and pain associated with genital sores.

⏱️ Dosage and Administration 57 words ▾

Directions Adults and children 12 years and over : • wash hands before applying ointment • apply to affected area at the first sign of blisters, sores or tingling sensation • rub in gently but completely • do not use more than 3 times a day. Children under the age of 12 years : Ask a doctor

⚠️ Warnings 102 words ▾

Warnings For external use only. This product is not a substitute for professional healthcare. Virally based infections are contagious.

This product will not stop the spread of the virus that causes Herpes or other viruses. Do not use • in the eyes • over large areas of the body • if you are allergic to any ingredients in this product. Ask a doctor before use if pregnant or nursing.

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days. Keep out of reach of children . If swallowed, call Poison Control or seek medical help.

🧪 Active Ingredient 59 words ▾

Active Ingredient Purpose Graphites 10X HPUS ..................................................Relief for skin eruptions in genital area Natrum Muriaticum 3X HPUS .......................................Blisters, itching and burning relief Symphytum Officinale (Comfrey) 1X HPUS.....................Inflammatory relief Thuja Occidentalis 3X HPUS ........................................Skin eruptions, itching and burning pain relief The letters HPUS indicate the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

🧪 Inactive Ingredients 25 words ▾

Inactive Ingredients beeswax, coconut oil (organic), cottonseed oil, eucalyptus oil, jojoba oil, lemongrass oil, lysine, magnesium oxide, MCT oil, peppermint oil, silver stearate, zinc oxide

📄 Package Label / Principal Display Panel 4 words ▾

Product label image description

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

About homeopathic listings

HerpaOne GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/g; 3 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g OINTMENT 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 it is currently marketed — but Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions has reported a marketing end date of 2027-01-08, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions 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.
← 24909-0060-28 · Aidance 24909-0062-14 · Aidance →
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.