Home › NDC Lookup › Ingredients › Eriodictyon Californicum, Histaminum, Ip... › 65808-0320-01
Real Relief Eriodictyon californicum, Histaminum, Ipecacuanha, Lobelia inflata, Sambucus nigra, Solidago virgaurea 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1 Tablet, 90-count — NDC 65808-0320-01 package photo

Real Relief Eriodictyon californicum, Histaminum, Ipecacuanha, Lobelia inflata, Sambucus nigra, Solidago virgaurea 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1 Tablet, 90-count

by GMP Laboratories of America, Inc. · 1 BOTTLE in 1 CARTON (65808-320-01) / 90 TABLET in 1 BOTTLE
NDC 65808-0320-01
🏷️ FDA NDC (as labeled) 65808-320-01 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) 65808-320-01
Product NDC 65808-320
11-digit billing NDC 65808032001
UNII 2Y7TIQ135H, 3POA0Q644U, 62I3C8233L, 9PP1T3TC5U, CT03BSA18U, 5405K23S50
SPL Set ID b79f7319-1ecc-77f5-e053-2a95a90a5a81
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-01-01
Route ORAL
Dosage form TABLET
Substance ERIODICTYON CALIFORNICUM LEAF; HISTAMINE DIHYDROCHLORIDE; IPECAC; LOBELIA INFLATA; SAMBUCUS NIGRA FLOWERING TOP; SOLIDAGO VIRGAUREA FLOWERING TOP
Why two NDCs? The FDA registers this code as 65808-320-01 — 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 → 65808-0320-01. 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

LabelerGMP Laboratories of America, Inc.
Labeler code65808
First marketedJan 2020
Product typeHuman Otc Drug
Portfolio5 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 is an oral tablet containing six plant-derived and chemical substances prepared according to homeopathic principles. The formula includes eriodictyon californicum leaf, lobelia inflata, sambucus nigra flowering top, and solidago virgaurea flowering top, which in homeopathic practice are traditionally associated with respiratory and upper respiratory tract symptoms. Histamine dihydrochloride and ipecac are also included in homeopathic dilutions. Homeopathic products are marketed based on traditional use and homeopathic theory; the FDA does not evaluate homeopathic drugs for effectiveness or safety.

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 white
ShapeRound
ImprintHLB
Size9 mm
ScoringNot scored
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 EWQ57Q8I5X
    Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.

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

The official label also statesInactive ingredients Lactose, Magnesium Stearate.

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 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
Real Relief 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]this 65808-0320-01 GMP 90 tablets — — FDA listed —
Real Relief 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X] 71971-6001-00 Homeolab 90 tablets — — 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

🏛️
2020
On the market since
Jan 2020
📍
2026
Currently FDA-listed
6 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
65808-0320-01 You're viewing this 1 BOTTLE in 1 CARTON (65808-320-01) / 90 TABLET in 1 BOTTLE 2020-01-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Real Relief Eriodictyon californicum, Histaminum, Ipecacuanha, Lobelia inflata, Sambucus nigra, Solidago virgaurea 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1; 8 [hp_X]/1 TABLET 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 65808-320-01, 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: 65808-0320-01, written without dashes as 65808032001. 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 65808-0320-01, the first segment (65808) is the labeler code FDA assigned to GMP Laboratories of America, Inc.; the middle segment (0320) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 GMP Laboratories of America, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
GMP Laboratories of America, 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 29 words ▾

Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve symptoms associated with asthma: gasping for air difficulty breathing wheezing coughing excess mucus

⏱️ Dosage and Administration 66 words ▾

Directions Chew tablets and let dissolve in mouth. Do not use more than directed. Do not take with food. Repeat 4 times daily and reduce intake with improvement or as directed by a health professional Age…………………………………………………………........ Dose Adults and Children 12 years of age and older………...... 2 tablets Children 2 to 11 years of age…...……………………............ 1 tablet Children under 2 years of age……………………................. Ask a doctor

⚠️ Warnings 29 words ▾

Warnings Stop use and ask a doctor if symptoms worsen or last for more than 7 days. If you are pregnant or breastfeeding, ask a health professional before use.

📦 Storage and Handling 15 words ▾

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

🧪 Active Ingredient 33 words ▾

Active Ingredients HPUS: Eriodictyon californicum (Yerba santa) 8 [hp_X] Histaminum 8 [hp_X] Ipecacuanha (Ipecac) 8 [hp_X] Lobelia inflata (Indian tobacco) 8 [hp_X] Sambucus nigra (European elder) 8 [hp_X] Solidago virgaurea (Goldenrod) 8 [hp_X]

🧪 Inactive Ingredients 5 words ▾

Inactive ingredients Lactose, Magnesium Stearate.

🎯 Purpose 51 words ▾

Purpose Homeopathic remedy helps relieve symptoms of asthma: gasping for air difficulty breathing wheezing coughing excess mucus The letters 'HPUS' indicate that the components in this product are officially monographed in the Homoeopathic Pharmacopoeia of the United States. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 65808-0318-01 · GMP 65808-0322-01 · GMP →
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.