Prid Ichthammol, Calcium Sulfide, Calendula Officinalis Flowering Top, Arnica Montana, Echinacea Angustifolia, Silicon Dioxide, Sulfur 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/g Salve — NDC 54973-4099-02 package photo

Prid Ichthammol, Calcium Sulfide, Calendula Officinalis Flowering Top, Arnica Montana, Echinacea Angustifolia, Silicon Dioxide, Sulfur 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/g Salve

by Hyland's Inc. · 1 CAN in 1 CARTON (54973-4099-2) / 18 g in 1 CAN
NDC 54973-4099-02
🏷️ FDA NDC (as labeled) 54973-4099-2 billing pads the package segment with a zero
This package
Contains18 g in 1 can Pack sizes2 compare ↓
Also comes in: 18 g 54973-4099-01
OTC On market Non-controlled
🗂️ Data synced Sep 3, 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) 54973-4099-2
Product NDC 54973-4099
11-digit billing NDC 54973409902
UNII 1MBW07J51Q, ETJ7Z6XBU4, VB06AV5US8, O80TY208ZW, 18E7415PXQ, NQ14646378 +1 more
UPC 0354973413016, 0354973415614, 0354973406919
SPL Set ID 49689eeb-7790-07f1-e063-6294a90a2df2
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-03-01
Route TOPICAL
Dosage form SALVE
Substance CALCIUM SULFIDE; SILICON DIOXIDE; ECHINACEA ANGUSTIFOLIA; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; ICHTHAMMOL; SULFUR
Why two NDCs? The FDA registers this code as 54973-4099-2 — 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 → 54973-4099-02. 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

LabelerHyland's Inc.
Labeler code54973
First marketedMar 2022
Product typeHuman Otc Drug
Portfolio69 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?

Prid Ichthammol is a topical salve marketed as a homeopathic product. It contains ichthammol, sulfur, calcium sulfide, and several plant extracts (arnica montana, calendula officinalis, and echinacea angustifolia) along with silicon dioxide. In homeopathic tradition, these ingredients are used to support skin health and comfort. This is an unapproved homeopathic product marketed based on homeopathic use and tradition, not evaluated by the FDA for effectiveness.

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 brown
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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 88S87KL877
    Rosin is a sticky resin extracted from pine trees. It's used in medicines as a binder and adhesive to help hold tablet ingredients together and improve how the medicine sticks to surfaces.
  • UNII 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • 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.

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

The official label also statesBeeswax, Ethyl Alcohol, Glycerine, Petrolatum, Purified Water, Stearyl Alcohol, Wood Rosin.

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.
Try another pack size: 18 g
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
Prid 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/g 54973-4069-01 Hyland's 1 can FDA listed
Prid 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/gthis 54973-4099-02 Hyland's 1 can 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

🏛️
2022
On the market since
Mar 2022
📍
2026
Currently FDA-listed
4 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Prid (this brand).

Top reported reactions

Abdominal Pain1
Application Site Erythema1
Application Site Pain1
Cellulitis1
Dizziness1
Erythema1
Headache1

Reporter sex

4 reports
Male · 50%
Female · 50%

Serious outcomes

Life-threatening2
Hospitalization1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
54973-4099-02 You're viewing this 1 CAN in 1 CARTON (54973-4099-2) / 18 g in 1 CAN 2026-04-22 Active
54973-4099-01 1 CAN in 1 CARTON (54973-4099-1) / 18 g in 1 CAN 2026-09-01 Active

Pack size FAQ

What quantity is in NDC 54973-4099-02?
NDC 54973-4099-02 is listed by the FDA — 1 can in 1 carton / 18 g in 1 can.
What NDC number is used to bill for this package of Prid Ichthammol, Calcium Sulfide, Calendula Officinalis Flowering Top, Arnica Montana, Echinacea Angustifolia, Silicon Dioxide, Sulfur 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/g Salve?
Bill NDC 54973-4099-02 — the 11-digit billing format is 54973409902. 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

Prid Ichthammol, Calcium Sulfide, Calendula Officinalis Flowering Top, Arnica Montana, Echinacea Angustifolia, Silicon Dioxide, Sulfur 12 [hp_X]/g; 12 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 2 [hp_X]/g; 12 [hp_X]/g SALVE 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 54973-4099-2, 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: 54973-4099-02, written without dashes as 54973409902. 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 54973-4099-02, the first segment (54973) is the labeler code FDA assigned to Hyland's Inc.; the middle segment (4099) 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 Hyland's Inc.. 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 1 other package presentation of this same product, including 1 can (54973-4099-01). 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?
Hyland's Inc. 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 30 words

Uses May help draw out splinters & ingrown hairs and temporarily relieve pain, itchiness and irritation from: ■ boils ■ minor skin eruptions ■ bites ■ superficial cuts or scratches

⏱️ Dosage and Administration 95 words

Directions Adults and children 6 years and over ■ Wash affected area with warm water, dry, and apply PRID® twice daily on affected area and cover with a clean bandage until irritation subsides. ■ Do not squeeze or pressure irritated skin. ■ Do not use other than directed

Adults and children 6 years and over ■ Wash affected area with warm water, dry, and apply PRID® twice daily on affected area and cover with a clean bandage until irritation subsides. ■ Do not squeeze or pressure irritated skin. ■ Do not use other than directed

⚠️ Warnings 69 words

Warnings For External Use Only. Do not use ■ in eyes, mouth and nose. ■ on deep puncture wounds. ■ on animal bites. ■ on serious burns. Stop use and ask a doctor if ■ symptoms persist for more than 7 days or worsen. ■ irritation, pain, swelling or redness persists or worsens. If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children.

🧪 Active Ingredient 83 words

Active ingredients Purpose Arnica Montana 3X HPUS eases pain and swelling Calendula Officinalis 3X HPUS eases pain from white hard bites Echinacea Angustifolia 3X HPUS eases pain from itchy red bites Hepar Sulph Calc 12X HPUS relieves pain from boils, itching Ichthammol 2X HPUS helps to heal the skin Silicea 12X HPUS helps to draw out splinters, thorns and ingrown hairs under the skin Sulphur 12X HPUS relieves itchiness, sores and minor skin eruptions "HPUS" is the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 13 words

Inactive ingredients Beeswax, Ethyl Alcohol, Glycerine, Petrolatum, Purified Water, Stearyl Alcohol, Wood Rosin.

🎯 Purpose 25 words

May help draw out splinters & ingrown hairs and temporarily relieve pain, itchiness and irritation from: boils, minor skin eruptions, bites superficial cuts or scratches

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.