NDC 17089-0451-23 — GUNA-SINUS NOSE ALTHAEA OFFICINALIS LEAF

🆔 Identity & classification

FDA NDC (as labeled) 17089-451-23

Product NDC 17089-451

11-digit billing NDC 17089045123

UNII 492225Q21H, E2QQV92338, 95IT3W8JZE, PQ6CK8PD0R, 9755T40D11, D1YM0P5Z2T +12 more

UPC 0317089451235

SPL Set ID 36fef678-17c6-4d2a-a0f0-ddb298611f25

Established class (EPC) Non-Standardized Food Allergenic Extract; Vitamin C; Copper-containing Intrauterine Device

Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Decreased Embryonic Implantation; Decreased Sperm Motility; Inhibit Ovum Fertilization

Chemical class Allergens; Dietary Proteins; Vegetable Proteins; Ascorbic Acid; Copper

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2010-05-27

Route NASAL

Dosage form SPRAY

Substance ONION; ALTHAEA OFFICINALIS LEAF; SILVER NITRATE; ASCORBIC ACID; BLACK CURRANT; LOBARIA PULMONARIA; COPPER; ECHINACEA ANGUSTIFOLIA; CALCIUM SULFIDE; GOLDENSEAL; POTASSIUM DICHROMATE; LACHESIS MUTA VENOM; MANGANESE; MERCURIC SULFIDE; SUS SCROFA NASAL MUCOSA

Why two NDCs? The FDA registers this code as 17089-451-23 — 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 → 17089-0451-23. 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

LabelerGuna spa

Labeler code17089

First marketedMay 2010

Product typeHuman Otc Drug

Portfolio83 products on file

🔎 All NDCs from Guna spa

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?

Guna-Sinus Nose is a nasal spray containing a blend of botanical extracts, minerals, and homeopathic ingredients. This is an unapproved homeopathic product marketed based on homeopathic tradition rather than FDA evaluation for effectiveness. The formula includes plant materials such as echinacea, goldenseal, and plantago, which are traditionally used in herbal practice, along with vitamin C and various mineral constituents. Homeopathic products are prepared according to homeopathic methods and are not evaluated by the FDA to establish safety or effectiveness.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

0.6 mL / 30 mL UNII 5A9KE2L9L3
A citrus fruit liquid used as a flavoring and vehicle in oral medicines. It adds natural taste, helps mask bitter drug flavors, and provides liquid volume for dissolving or suspending active ingredients.
0.03 mL / 30 mL 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.
0.03 mL / 30 mL 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.
15.9 mL / 30 mL 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 statesInactive ingredient: orange juice, potassium sorbate, sodium benzoate, water.

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 system	Per mL	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Guna-Sinus Nose 8 [hp_X]/30mL; 2 [hp_X]/30mL; 10 [hp_X]/30mL; 2 [hp_X]/30mL; 1 [hp_X]/30mL; 2 [hp_X]/30mL; 3 [hp_X]/30mL; 3 [hp_X]/30mLthis 17089-0451-23	Guna	1 bottle	—	—	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

🏛️

2010

On the market since

May 2010

📍

2026

Currently FDA-listed

16 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 NDC	Description	Marketing start	Status
17089-0451-23 You're viewing this	1 BOTTLE, SPRAY in 1 BOX (17089-451-23) / 30 mL in 1 BOTTLE, SPRAY	2018-12-21	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

GUNA-SINUS NOSE ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA 8 [hp_X]/30mL; 2 [hp_X]/30mL; 10 [hp_X]/30mL; 2 [hp_X]/30mL; 1 [hp_X]/30mL; 2 [hp_X]/30mL; 3 [hp_X]/30mL; 3 [hp_X]/30mL SPRAY 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 17089-451-23, 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: 17089-0451-23, written without dashes as 17089045123. 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 17089-0451-23, the first segment (17089) is the labeler code FDA assigned to Guna spa; the middle segment (0451) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (23) 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 Guna spa. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

Guna spa 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 25 words ▾

Directions : tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.

⏱️ Dosage and Administration 48 words ▾

DIRECTIONS Adults and children 12 years and older 2 sprays to each nostril, 3-5 times per day Children between 12 years and 6 years of age 1 spray to each nostril, 3-5 times per day Children under 6 years 1 spray to each nostril, 3 times per day

⚠️ Warnings 44 words ▾

WARNINGS Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 117 words ▾

ACTIVE INGREDIENTS/PURPOSE ALIUM CEPA 6X, 8X, 12X EXPECTORANT ALTHEA OFFICINALIS 2X EXPECTORANT ARGENTUM NITRICUM 10X HEADACHE ANALGESIC ASCORBIC ACID 2X ANTIOXIDANT BLACK CURRANT 1X DETOXIFICATION COMMON LUNGWORT 2X DECONGESTANT CUPRUM METALLICUM 3X ANTIVIRAL IMMUNE SUPPORT ECHINACEA ANGUSTIFOLIA 3X ANTIBACTERIAL IMMUNE SUPPORT HEPAR SULFURIS CALCAREUM 6X, 8X, 12X ANTIOXIDANT HYDRASTIS CANADENSIS 6X, 8X, 12X MUCOLYTIC KALI BICHROMICUM 6X, 8X, 12X MUCOLYTIC LACHESIS MUTUS 12X, 30X, 200X DECONGESTANT MANGANUM METALLICUM 3X DECONGESTANT MERCURIUS SULPHURATUS RUBER 6X, 8X, 12X ANTI-INFLAMMATORY MUCOSA NASALIS 6X, 12X, 30X SUPPORTS IMMUNE RESPONSE PLANTAGO MAJOR 2X DETOXIFICATION PULSATILLA 6X, 8X, 12X DECONGESTANT SILICEA 6X, 8X, 12X DECONGESTANT SINUSITISINUM 12X, 30X DECONGESTANT THYMUS GLAND 6X, 12X, 30X SUPPORTS IMMUNE RESPONSE URINARY BLADDER 10X, 30X, 200X DETOXIFICATION

🧪 Inactive Ingredients 9 words ▾

Inactive ingredient: orange juice, potassium sorbate, sodium benzoate, water.

🎯 Purpose 21 words ▾

USES For the temporary relief of symptoms due to acute and chronic Sinus Infection: Sinus Headaches Post Nasal Drip Nasal Congestion

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

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