Home › NDC Lookup › Ingredients › Onion, Galphimia Glauca Flowering Top, H... › 62795-4006-09
👃image loading
(from DailyMed)

Clearlife Extra Strength ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA and SCHOENOCAULON OFFICINALE SEED 4 [hp_X]/20mL; 4 [hp_X]/20mL; 8 [hp_X]/20mL; 3 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mL Spray

by MediNatura Inc. · 1 BOTTLE, PUMP in 1 CARTON (62795-4006-9) / 20 mL in 1 BOTTLE, PUMP
NDC 62795-4006-09
🏷️ FDA NDC (as labeled) 62795-4006-9 billing pads the package segment with a zero
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

🚨
Active recall for this product.
Class I · Dec 12, 2025 — Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. (Medinatura New Mexico, inc.) · FDA recall D-0289-2026
Check your lot/expiration against the official notice — look up the recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 62795-4006-9
Product NDC 62795-4006
11-digit billing NDC 62795400609
NCPDP billing unit ML — per mL (volume)
UNII 492225Q21H, 93PH5Q8M7E, 3POA0Q644U, C4MO6809HU, 70FD1KFU70, 9W34L2CQ9A +2 more
SPL Set ID 09fbebf9-3d8b-479c-80f3-37f07cb699d6
Established class (EPC) Non-Standardized Food Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Vegetable Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-06
Route NASAL
Dosage form SPRAY
Substance ONION; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR; AMBROSIA ARTEMISIIFOLIA WHOLE; EUPHRASIA STRICTA; SCHOENOCAULON OFFICINALE SEED
GPI-14 99870010000950
GPI class ClearLife Allergy Nasal
Why two NDCs? The FDA registers this code as 62795-4006-9 — 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 → 62795-4006-09. 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

LabelerMediNatura Inc.
Labeler code62795
First marketedJan 2021
Product typeHuman Otc Drug
Portfolio4 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 an unapproved homeopathic nasal spray containing eight plant and mineral ingredients. In homeopathic practice, these ingredients (onion, galphimia glauca, luffa, euphrasia, ambrosia artemisiifolia, sulfur, schoenocaulon officinale, and histamine) are traditionally used to address allergy-like symptoms. Homeopathic products are marketed based on homeopathic tradition rather than scientific evidence and are not evaluated by the FDA 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.

🧪 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 F5UM2KM3W7
    Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII 94255I6E2T
    Sodium phosphate dibasic dihydrate is a salt that helps control the acidity level of a medicine. It acts as a buffer and pH regulator to keep the medication stable and effective.
  • UNII 5QWK665956
    A salt derived from phosphoric acid and sodium, used primarily as a buffer to control the acidity or pH of a medication, helping keep it stable during storage and use.

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

The official label also statesBenzalkonium chloride, Disodium phosphate dihydrate, Isotonic sodiumchloride solution, Sodium dihydrogen phosphate dihydrate

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.
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
Clearlife Extra Strength 4 [hp_X]/20mL; 4 [hp_X]/20mL; 8 [hp_X]/20mL; 3 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mLthis 62795-4006-09 MediNatura 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

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 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
62795-4006-09 You're viewing this 1 BOTTLE, PUMP in 1 CARTON (62795-4006-9) / 20 mL in 1 BOTTLE, PUMP 2021-01-06 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Clearlife Extra Strength ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA and SCHOENOCAULON OFFICINALE SEED 4 [hp_X]/20mL; 4 [hp_X]/20mL; 8 [hp_X]/20mL; 3 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mL; 4 [hp_X]/20mL 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 — 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 62795-4006-9, 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: 62795-4006-09, written without dashes as 62795400609. 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 62795-4006-09, the first segment (62795) is the labeler code FDA assigned to MediNatura Inc.; the middle segment (4006) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) 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 MediNatura Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
MediNatura 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 32 words ▾

INDICATIONS AND USAGE For the temporary relief of minor allergy symptoms:Sinus pressure, Runny or itchy nose, Nasal congestion, Allergic rhinitis, sneezing, itchy or watery eyes, Allergic related headache, itchy throat or skin.

⏱️ Dosage and Administration 86 words ▾

Directions: Adults and children 12 years and older: During an allergy attack: 2 sprays into each nostril every 2-4 hours. For daily protection:2 sprays into each nostril daily. Do not exceed 24 sprays in each nostril per 24 hours.

Children 4 to 11 years: During an allergy attack:1 spray into each nostril every 2 to 4 hours. For daily protection 1 spray into each nostril daily. Do not exceed 12 sprays in each nostril per 24 hours.

For children under 4 years, consult your health professional.

⚠️ Warnings 83 words ▾

WARNINGS Ask a doctor before use if you have asthma. In rare cases broncho-spasm may occur in asthmatic patients. Temporary burning, stinging, sneezing or increased nasal discharge may occur.

If pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children. The use of this dispenser by more than one person may spread infection.

If symptoms persist or worsen, a healthcare professional should be consulted. Do not use if known sensitivity to ClearLife™ or any of its ingredients exists.

🧪 Active Ingredient 39 words ▾

ACTIVE INGREDIENTS *Allium cepa 4X, 12X, 20X, Ambrosia Artemisiaefolia 4X,12X, 20X, Euphrasia Officinalis 4X, 12X, 20X, *Galphimia glauca 4X, 12X, 20X *Histaminum hydrochloricum 8X,12X, 20X, *Luffa operculate 3X,12X, 20X, Sabadilla 4X, 12X, 20X, *Sulphur 4X, 12X, 20X *Natural Ingredients.

🧪 Inactive Ingredients 14 words ▾

INACTIVE INGREDIENTS Benzalkonium chloride, Disodium phosphate dihydrate, Isotonic sodiumchloride solution, Sodium dihydrogen phosphate dihydrate

🎯 Purpose 27 words ▾

PURPOSE Relieves: • Runny or itchy Nose • Sneezing • Nasal Congestion • Sinus pressure • Allergic rhinitis • itchy or watery eyes • Allergic related headache

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 62795-4005-09 · MediNatura 62795-6050-07 · Medinatura →
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.