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30C Homeopathic Remedy Kit 50 Kit

by Washington Homeopathic Products · 50 VIAL, GLASS in 1 KIT (71919-821-18) / 1 KIT in 1 VIAL, GLASS (71919-821-01) * 750 PELLET in 1 VIAL, GLASS (68428-127-01) * 750 PELLET in 1 VIAL, GLASS (68428-124-01) * 750 PELLET in 1 VIAL, GLASS (68428-123-01) * 750 PELLET in 1 VIAL, GLASS (6
NDC 71919-0821-18
🏷️ FDA NDC (as labeled) 71919-821-18 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 →

This page is curated, coded, and maintained by

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

🆔 Identity & classification

FDA NDC (as labeled) 71919-821-18
Product NDC 71919-821
11-digit billing NDC 71919082118
UPC 0740640642986
SPL Set ID 11e5ee81-1391-0dd3-e063-6294a90a5d0b
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-21
Route ORAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 71919-821-18 — 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 → 71919-0821-18. 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

LabelerWashington Homeopathic Products
Labeler code71919
First marketedFeb 2024
Product typeHuman Otc Drug
Portfolio49 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 remedy kit containing 50 oral doses formulated at 30C potency. Homeopathic products are marketed based on traditional homeopathic practice and are not evaluated by the FDA for safety or effectiveness. The specific remedies in this kit are used in homeopathic tradition to address various minor complaints, though the active ingredients are not listed on this package. Homeopathic products are considered unapproved drugs under FDA classification.

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.

🧪 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.

From the label’s inactive-ingredient sectionSucrose/Lactose

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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
30C Homeopathic Remedy Kitthis 71919-0821-18 Washington 50 vials — — 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

🏛️
2024
On the market since
Feb 2024
📍
2026
Currently FDA-listed
2 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
71919-0821-18 You're viewing this 50 VIAL, GLASS in 1 KIT (71919-821-18) / 1 KIT in 1 VIAL, GLASS (71919-821-01) * 750 PELLET in 1 VIAL, GLASS (68428-127-01) * 750 PELLET in 1 VIAL, GLASS (68428-124-01) * 750 PELLET in 1 VIAL, GLASS (68428-123-01) * 750 PELLET in 1 VIAL, GLASS (6 2024-02-21 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing Kit / multi-component package

About homeopathic listings

30C Homeopathic Remedy Kit 50 KIT 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.

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 — Not published for this NDC No photo available yet for this listing.
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 71919-821-18, 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: 71919-0821-18, written without dashes as 71919082118. 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 71919-0821-18, the first segment (71919) is the labeler code FDA assigned to Washington Homeopathic Products; the middle segment (0821) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (18) 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 Washington Homeopathic Products. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Washington Homeopathic 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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 144 words ▾

INDICATIONS Acon nap fear Aesculus hipp hemorrhoids Allium cepa head cold Antimon crud warts Apis mel stings Arnica bruises Arsenicum alb vomiting Belladonna fever Bellis bruised soreness Berber vulg itching Bryonia worse motion Calc carb overwork Caulophyllum cramps Causticum hoarseness Chamomilla irritability Cimicifuga minor back pain Coffea cruda sleeplessness Drosera cough Eupatorium perf flu-like symptoms Euphrasia eye irritation Ferrum phos low fever Gelsemium lethargy Hamamelis varicose veins Hepar sulph calc croupiness Hydrastis sinuses Hypericum shooting pain Ignatia sadness Ipecac nausea Kali bic sinuses Kali carb sour belching Kali mur congested ears Kali phos irritability Lachesis sore throat Ledum black eyes Lycopodium digestion Mag phos cramps Nat mur sneezing Nux vom vomiting Petroleum nausea Phosphoricum ac headache Phytolacca sore throat Podoph pelt diarrhea Pulsatilla weeping Rhus tox better motion Ruta bruised feeling Sepia indifference Staphysag anger Sulphur skin problems Symphytum prickling pain Thuja occ warts

⏱️ Dosage and Administration 53 words ▾

DIRECTIONS Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by a licensed practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by a licensed practitioner. Take at greater intervals as condition subsides.

⚠️ Warnings 19 words ▾

STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant or nursing, stop use and consult your practitioner.

🧪 Active Ingredient 76 words ▾

ACTIVE INGREDIENTS Acon nap Aesculus hipp Allium cepa Antimon crud Apis mel Arnica Arsenicum alb Belladonna Bellis Berber vulg Bryonia Calc carb Caulophyllum Causticum Chamomilla Cimicifuga Coffea cruda Drosera Eupatorium perf Euphrasia Ferrum phos Gelsemium Hamamelis Hepar sulph calc Hydrastis Hypericum Ignatia Ipecac Kali bic Kali carb Kali mur Kali phos Lachesis Ledum Lycopodium Mag phos Nat mur Nux vom Petroleum Phosphoricum ac Phytolacca Podoph pelt Pulsatilla Rhus tox Ruta Sepia Staphysag Sulphur Symphytum Thuja occ

🧪 Inactive Ingredients 3 words ▾

INACTIVE INGREDIENTS Sucrose/Lactose

🎯 Purpose 75 words ▾

USES To relieve symptoms of fear, hemorrhoids, head cold, warts, stings, bruises, vomiting, fever, bruised soreness, itching, worse motion, oberwork, cramps, hoarseness, irritability, minor back pain, sleeplessness, cough, flu-like symptoms, eye irritation, low fever, lethargy, varicose veins, croupiness, sinuses, shooting pain, sadness, nausea, sinuses, sour belching, congested ears, irritability, sore throat, black eyes, digestion, cramps, sneezing, vomiting, nausea, headache, sore throat, diarrhea, weeping, better motion, bruised feeling, indifference, anger, skin problems, prickling pain, and warts.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 71919-0820-01 · Washington 71919-0822-18 · Washington →
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.