ReBoost SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE and PULSATILLA VULGARIS 10 [hp_X]/20mL; 4 [hp_X]/20mL; 10 [hp_X]/20mL; 5 [hp_X]/20mL; 6 [hp_X]/20mL; 2 [hp_X]/20mL; 6 [hp_X]/20mL Spray
by MediNatura · 1 BOTTLE, PUMP in 1 CARTON (62795-4005-9) / 20 mL in 1 BOTTLE, PUMP
NDC 62795-4005-09
🏷️ FDA NDC (as labeled)
62795-4005-9
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 →
🚨
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-0288-2026
Check your lot/expiration against the official notice — look up the recall number in the FDA recall database ↗
🆔 Identity & classification
FDA NDC (as labeled)
62795-4005-9
Product NDC
62795-4005
11-digit billing NDC
62795400509
NCPDP billing unit
ML — per mL (volume)
UNII
95IT3W8JZE, 1TI1O9028K, 1MBW07J51Q, ZW3Z11D0JV, T4423S18FM, C4MO6809HU +4 more
SPL Set ID
cb8a8d2a-d9d2-4a71-9279-c5641a9126c6
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-02-04
Route
NASAL
Dosage form
SPRAY
Substance
SILVER NITRATE; EUPHORBIA RESINIFERA RESIN; CALCIUM SULFIDE; GOLDENSEAL; POTASSIUM DICHROMATE; LUFFA OPERCULATA FRUIT; SODIUM CARBONATE; PULSATILLA VULGARIS; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; ECHINACEA, UNSPECIFIED
GPI-14
99870010000950
GPI class
ReBoost Breathe Easy
Why two NDCs?
The FDA registers this code as 62795-4005-9 — 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 → 62795-4005-09. 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
Labeler code62795
First marketedFeb 2020
Product typeHuman Otc Drug
Portfolio2 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 a nasal spray marketed as a homeopathic product containing multiple ingredients including silver nitrate, goldenseal, echinacea, and pulsatilla vulgaris, among others. In homeopathic practice, these ingredients are traditionally used to support respiratory and immune function, though homeopathic products are based on traditional use rather than clinical evidence. This product is not evaluated by the FDA for effectiveness. The specific potencies listed indicate this follows homeopathic preparation methods.
Patient education
Supplement & herbal interactions
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.
💬 Questions about SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE and PULSATILLA VULGARIS?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.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 |
|---|---|---|---|---|---|---|
| ReBoost 10 [hp_X]/20mL; 4 [hp_X]/20mL; 10 [hp_X]/20mL; 5 [hp_X]/20mL; 6 [hp_X]/20mL; 2 [hp_X]/20mL; 6 [hp_X]/20mLthis 62795-4005-09 | 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
🏛️
2020
On the market since
Feb 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.
🔬 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 APIS MELLIFERA, ATROPA BELLADONNA, ZINC GLUCONATE, BAPTISIA TINCTORIA ROOT, ULMUS RUBRA BARK, SULFUR, ZINC ACETATE ANHYDROUS,VINCETOXICUM HIRUNDINARIA ROOT and CAIRINA MOSCHATA HEART/LIVER — the ingredient across all brands.
Top reported reactions
Reporter sex
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 62795-4005-09 You're viewing this | 1 BOTTLE, PUMP in 1 CARTON (62795-4005-9) / 20 mL in 1 BOTTLE, PUMP | 2020-02-04 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
Homeopathic listing
About homeopathic listings
ReBoost SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE and PULSATILLA VULGARIS 10 [hp_X]/20mL; 4 [hp_X]/20mL; 10 [hp_X]/20mL; 5 [hp_X]/20mL; 6 [hp_X]/20mL; 2 [hp_X]/20mL; 6 [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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 62795-4005-9, 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: 62795-4005-09, written without dashes as 62795400509. 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 62795-4005-09, the first segment (62795) is the labeler code FDA assigned to MediNatura; the middle segment (4005) 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. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
MediNatura 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 ▾
Uses Uses: To temporarily relieve nasal congestion. To reduce cold and flu symptoms such as sinus headache & pressure.
⏱️ Dosage and Administration ▾
DIRECTIONS Directions: Adults and children 12 years and older: 2 sprays into each nostril every 2-4 hours. Do not exceed 24 sprays in each nostril in 24 hours. Children 4 to 11 years: 1 spray into each nostril every 2-4 hours. Do not exceed 12 sprays into each nostril in 24 hours. For children under 4 years, consult your health professional.
⚠️ Warnings ▾
WARNINGS Warnings: Ask a doctor before use if you have asthma. In rare cases bronchospasm may occur in asthmatic patients. Temporary burning, stinging, sneezing, or increased nasal discharge may occur.
If pregnant or breast-feeding, ask a health 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 health professional should be consulted. Do not use if known sensitivity to ReBoost™ or any of its ingredients exists.
🧪 Active Ingredient ▾
ACTIVE INGREDIENTS Anas barbariae 20X, 200C 1% *Luffa operculata 2X 1% *Pulsatilla 2X 1% *Organic Echinacea 3X 1% *Euphorbium officinarum 4X 1% *Hydrastis canadensis 5X 1% Kali bichromicum 6X 1% Natrum carbonicum 6X 1% Argentum nitricum 10X 1% *Hepar sulphuris calcareum 10X 1%
🧪 Inactive Ingredients ▾
INACTIVE INGREDIENTS Inactive Ingredients: Benzalkonium chloride, Disodium phosphate dihydrate, Isotonic sodium chloride solution, Sodium dihydrogen phosphate dihydrate
🎯 Purpose ▾
PURPOSE Relieves nasal congestion Relieves post nasal drip Relieves sneezing Relieves sinus headache & pressure Relieves runny nose Relieves nasal itching
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.