Home › NDC Lookup › Ingredients › Drosera, Arnica Montana, Bryonia, Cetrar... › 71971-9204-04
Real Relief DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CAMOMILLA, COFFEA CRUDEA 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/ Liquid, 30 mL — NDC 71971-9204-04 package photo

Real Relief DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CAMOMILLA, COFFEA CRUDEA 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/ Liquid, 30 mL

by Homeolab International (Canada) inc · 30 mL in 1 BOTTLE (71971-9204-4)
NDC 71971-9204-04
🏷️ FDA NDC (as labeled) 71971-9204-4 billing pads the package segment with a zero
This package
Contains30 mL Pack sizes3 compare ↓
Also comes in: 100 mL 71971-9204-05 250 mL 71971-9204-09
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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) 71971-9204-4
Product NDC 71971-9204
11-digit billing NDC 71971920404
UNII 75O014T1HG, O80TY208ZW, 56K0VVT47P, BJ7YPN79A1, LZB7TFX1LT, 22Z32PWR7R +3 more
SPL Set ID fc6a509a-f4c0-47e7-8693-906ba6e03923
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Plant Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-03-03
Route ORAL
Dosage form LIQUID
Substance DROSERA ROTUNDIFOLIA FLOWERING TOP; ARNICA MONTANA; BRYONIA ALBA WHOLE; CETRARIA ISLANDICA SUBSP. ISLANDICA; PROTORTONIA CACTI; CORALLIUM RUBRUM WHOLE; TIN; CHAMOMILE; ARABICA COFFEE BEAN
Why two NDCs? The FDA registers this code as 71971-9204-4 — 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 → 71971-9204-04. 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

LabelerHomeolab International (Canada) inc
Labeler code71971
First marketedMar 2018
Product typeHuman Otc Drug
Portfolio23 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?

Real Relief Drosera is a homeopathic liquid taken by mouth that contains nine plant and mineral ingredients traditionally used in homeopathic practice. The formula includes drosera (sundew plant), arnica montana, bryonia, chamomile, and other botanical extracts, along with tin, which practitioners have used in homeopathic formulations for respiratory and cough-related concerns. Homeopathic products are based on traditional use and are not evaluated by the FDA for safety or effectiveness. This product is marketed under homeopathic principles rather than as a conventional medicine.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII T9D99G2B1R
    Caramel is a brown coloring substance made by heating sugar. It's added to medicines to give them color and sometimes a slight sweet taste without affecting how the drug works.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • 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.

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

The official label also statesInactive ingredients Purified water, sorbitol, caramel, sodium benzoate, potassium sorbate, citric acid

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: 100 mL 250 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
Real Relief 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/this 71971-9204-04 Homeolab 30 ml — — FDA listed —
Real Relief 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/ 63388-0920-44 Laboratoire 30 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

🏛️
2018
On the market since
Mar 2018
📍
2026
Currently FDA-listed
8 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
71971-9204-04 You're viewing this 30 mL in 1 BOTTLE (71971-9204-4) 2018-03-03 Active
71971-9204-05 1 BOTTLE in 1 CARTON (71971-9204-5) / 100 mL in 1 BOTTLE 2018-03-03 Active
71971-9204-09 1 BOTTLE in 1 CARTON (71971-9204-9) / 250 mL in 1 BOTTLE 2018-03-03 Active

Pack size FAQ

What quantity is in NDC 71971-9204-04?
NDC 71971-9204-04 contains 30 mL — 30 ml in 1 bottle.
What NDC number is used to bill for this package of Real Relief DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CAMOMILLA, COFFEA CRUDEA 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/ Liquid?
Bill NDC 71971-9204-04 — the 11-digit billing format is 71971920404. 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

Real Relief DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CAMOMILLA, COFFEA CRUDEA 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 1 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/100mL; 3 [hp_C]/ LIQUID 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 71971-9204-4, 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: 71971-9204-04, written without dashes as 71971920404. 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 71971-9204-04, the first segment (71971) is the labeler code FDA assigned to Homeolab International (Canada) inc; the middle segment (9204) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) 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 Homeolab International (Canada) 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 2 other package presentations of this same product, including 1 bottle (71971-9204-05), 1 bottle (71971-9204-09). 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?
Homeolab International (Canada) 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 ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 34 words ▾

Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve symptoms associated with nighttime cough and cold*: •dry cough •cough with expectoration •chest congestion •fever •aches and pains

⏱️ Dosage and Administration 70 words ▾

Directions •Do not exceed recommended dosage •Do not take with food •Take before bedtime. Repeat every 8 hours as needed and reduce with improvement or as directed by a health care professional. Age .....................................................................

Dose Adults and Children 12 + years...............................10 ml or 2 teaspoons (tsp) Children 6 to 11 years of age..................................5 ml or 1 teaspoon (tsp) Children 2 to 5 years of age....................................2.5 ml or 1/2 teaspoon (tsp)

⚠️ Warnings 68 words ▾

Warnings Stop use and ask a doctor if •Pain & cough gets worse or lasts more than 5 days •Fever gets worse or lasts more than 3 days •Redness or swelling is present •New symptoms occur •Cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition If you are pregnant or breastfeeding , ask a health professional before use.

📦 Storage and Handling 15 words ▾

Other information •do not use if seal is broken or missing •Store at room temperature.

🧪 Active Ingredient 63 words ▾

Active Ingredients HPUS : Drosera 1C (Sundew) Arnica montana 3C (Leopards Bane) Bryonia 3C (White Bryony) Cetraria islandica 1C (Iceland Moss) Coccus cacti 3C (Cochineal) Corallium rubrum 3C (Red Coral) Stannum metallicum 3C (Tin) Camomilla 4C (German Chamomille) Coffea crudea 4C (coffee) The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharcopoeia of the United States

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients Purified water, sorbitol, caramel, sodium benzoate, potassium sorbate, citric acid

🎯 Purpose 60 words ▾

Purpose Drosera 1C (Sundew)................................................dry cough Arnica montana 3C (Leopard's Bane)...........................aches and pains, chest congestion Bryonia 3C (White Bryony) .......................................painful cough Cetraria islandica 1C (Iceland Moss)...........................cough with expectoration Coccus cacti 3C (Cochineal)......................................cough with expectoration Corallium rubrum 3C (Red Coral)..............................painful cough Stannum metallicum 3C (Tin)...................................cough, chills, and lessens mucus Camomilla 4C (German Chamomille).........................restlessness, irritability, nocturnal awakenings Coffea crudea 4C (coffee)........................................restlessness and sleeplessness

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 71971-9185-04 · Homeolab 71971-9214-08 · Homeolab →
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.