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SINUS RX Calcarea carb, Euphorbium, Hydrastis, Kali bic, Kali iod, Lycopodium, Phosphorus, Pulsatilla, Thuja occ, Sanguinaria 9 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 9 [hp_X]/mL; 8 [hp_X]/mL; 6 [hp_X]/mL; 10 [hp_X]/mL Liquid, 30 mL — NDC 69390-0002-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

SINUS RX Calcarea carb, Euphorbium, Hydrastis, Kali bic, Kali iod, Lycopodium, Phosphorus, Pulsatilla, Thuja occ, Sanguinaria 9 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 9 [hp_X]/mL; 8 [hp_X]/mL; 6 [hp_X]/mL; 10 [hp_X]/mL Liquid, 30 mL — NDC 69390-002-01 (Billing 69390-0002-01)

by Miami Beach Pediatrics pa · 30 mL in 1 BOTTLE, DROPPER

This is a package of 30 mL of SINUS RX Calcarea carb, Euphorbium, Hydrastis, Kali bic, Kali iod, Lycopodium, Phosphorus, Pulsatilla, Thuja occ, Sanguinaria 9 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 9 [hp_X]/mL; 8 [hp_X]/mL; 6 [hp_X]/mL; 10 [hp_X]/mL Liquid from Miami Beach Pediatrics pa, marketed since Nov 2015 and currently FDA-listed. It is this product's only package size.

NDC 69390-0002-01
🏷️ FDA NDC (as labeled) 69390-002-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 69390-002-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69390 labeler · 002 product · 01 package
Package marketed since
Nov 22, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6939000201 9
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69390-002-01
Product NDC 69390-002
11-digit billing NDC 69390000201
UNII 2E32821G6I, 1TI1O9028K, ZW3Z11D0JV, T4423S18FM, 1C4QK22F9J, C88X29Y479 +4 more
SPL Set ID 078f6bfd-b4ff-4b20-8cff-83b7cd30f147
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-11-23
Route ORAL
Dosage form LIQUID
Substance OYSTER SHELL CALCIUM CARBONATE, CRUDE; EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; POTASSIUM DICHROMATE; POTASSIUM IODIDE; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; PULSATILLA VULGARIS; THUJA OCCIDENTALIS LEAFY TWIG; SANGUINARIA CANADENSIS ROOT
Why two NDCs? The FDA registers this code as 69390-002-01 — 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 → 69390-0002-01. 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.

Clinical

🧪 What is this product?

Sinus RX is an unapproved homeopathic liquid taken by mouth that contains multiple plant and mineral ingredients. In homeopathic practice, these ingredients are traditionally used to address sinus-related symptoms, though homeopathic products are based on homeopathic tradition and have not been evaluated by the FDA for effectiveness. The product includes substances such as goldenseal, potassium iodide, and thuja, which appear in various homeopathic preparations marketed for sinus and respiratory support.

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 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.
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
69390-0002-01 You're viewing this Main listing 30 mL in 1 BOTTLE, DROPPER 2017-11-22 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Sinus Rx 9 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 9 [hp_X]/mL; 8 [hp_X]/mL; 6 [hp_X]/mL; 10 [hp_X]/mLthis 69390-0002-01 Miami 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

🏛️
2015
On the market since
Nov 2015
📍
2026
Currently FDA-listed
11 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 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 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 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 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.

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

The official label also statesCitric Acid, Potassium Sorbate, Purified Water, Vegetable Glycerin.

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

LabelerMiami Beach Pediatrics pa
Labeler code69390
First marketedNov 2015
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Miami Beach Pediatrics pa labeler code 69390

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 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

USES: Temporarily relieves congestion and coughing due to sinusitis.

⏱️ Dosage and Administration 26 words ▾

DIRECTIONS: Shake well and take 5 drops under tongue 3 times a day for 10 days. Take at least 15 minutes away from eating or drinking.

⚠️ Warnings 43 words ▾

WARNINGS: This product is to be used under the supervision of your healthcare provider. If symptoms worsen or persist for more than 5 days, consult your practitioner. IF PREGNANT OR NURSING, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN.

🧪 Active Ingredient 50 words ▾

ACTIVE INGREDIENTS (HPUS*): Equal amounts of: Calcarea carb 9X, Euphorbium 6X, Hydrastis 6X, Kali bic 9X, Kali iod 8X, Lycopodium 6X, Phosphorus 10X, Pulsatilla 4X, Thuja occ 6X, Sanguinaria 9X. *The letters "HPUS" indicate the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

🧪 Inactive Ingredients 10 words ▾

INACTIVE INGREDIENTS: Citric Acid, Potassium Sorbate, Purified Water, Vegetable Glycerin.

🎯 Purpose 2 words ▾

Sinus Infections

📄 Keep Out of Reach of Children 6 words ▾

KEEP OUT OF REACH OF CHILDREN.

📄 Other Information 16 words ▾

OTHER INFORMATION: Do not use if cap seal is broken. Store in a cool, dry place.

📄 Questions or Comments 18 words ▾

QUESTIONS or COMMENTS? Miami Beach Pediatrics 975 41st Street, Suite #408 Miami Beach, FL 33140 Tel: 305-672-7337 www.miamibeachpediatrics.com

📄 Package Label / Principal Display Panel 27 words ▾

NDC: 69390-002-01 Dr. Eisenberg's SINUS RX Sinus Infections HOMEOPATHIC MEDICINE 1 fl oz (30 mL) MIAMI BEACH PEDIATRICS CENTER FOR INTEGRATIVE MEDICINE 1oz bottle label Sinus Infections

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 SINUS RX (this brand).

Top reported reactions

Chest Discomfort1
Chromaturia1
Dizziness1
Dyspnoea1
Haematochezia1
Muscle Spasms1
Pyrexia1

Reporter sex

1 reports
Male · 100%
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

SINUS RX Calcarea carb, Euphorbium, Hydrastis, Kali bic, Kali iod, Lycopodium, Phosphorus, Pulsatilla, Thuja occ, Sanguinaria 9 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 9 [hp_X]/mL; 8 [hp_X]/mL; 6 [hp_X]/mL; 10 [hp_X]/mL 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 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: this package is listed as actively marketed, with no marketing end date reported by Miami Beach Pediatrics pa. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Miami Beach Pediatrics pa 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.
← 69390-0001-01 · Miami 69395-0384-01 · A&C →
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.