![MDFARMA COLD and FLU RELIEF ATROPINE, NAJA NAJA VENOM, MAGNESIUM CHLORIDE, POTASSIUM HYDROXIDE 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 7 [hp_X]/.2mL Spray, 5 mL — NDC 73002-0713-03 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=8c2acd62-2f81-4dde-b258-870cd9469f6e&name=IMAGE-1.jpg)
MDFARMA COLD and FLU RELIEF ATROPINE, NAJA NAJA VENOM, MAGNESIUM CHLORIDE, POTASSIUM HYDROXIDE 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 7 [hp_X]/.2mL Spray, 5 mL
by Green Earth Health Inc. · 5 mL in 1 BOTTLE, SPRAY (73002-713-03)
NDC 73002-0713-03
🏷️ FDA NDC (as labeled)
73002-713-03
billing pads the product 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 →
🆔 Identity & classification
FDA NDC (as labeled)
73002-713-03
Product NDC
73002-713
11-digit billing NDC
73002071303
UNII
7C0697DR9I, ZZ4AG7L7VM, 02F3473H9O, WZH3C48M4T
SPL Set ID
8c2acd62-2f81-4dde-b258-870cd9469f6e
Established class (EPC)
Anticholinergic; Cholinergic Muscarinic Antagonist
Mechanism of action
Cholinergic Antagonists; Cholinergic Muscarinic Antagonists
DEA schedule
Non-controlled
Marketing category
UNAPPROVED DRUG OTHER
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-09-23
Marketing end
2026-09-30
Route
NASAL
Dosage form
SPRAY
Substance
ATROPINE; NAJA NAJA VENOM; MAGNESIUM CHLORIDE; POTASSIUM HYDROXIDE
Why two NDCs?
The FDA registers this code as 73002-713-03 — 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 → 73002-0713-03. 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
LabelerGreen Earth Health Inc.
Labeler code73002
First marketedSep 2020
Product typeHuman Otc Drug
Portfolio10 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 product containing atropine, magnesium chloride, naja naja venom, and potassium hydroxide, marketed for cold and flu relief. Atropine is an anticholinergic agent typically used to reduce certain secretions and muscle contractions. Magnesium chloride and potassium hydroxide are mineral salts found in various over-the-counter products. This product is marketed without an approved FDA application.
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 ATROPINE, NAJA NAJA VENOM, MAGNESIUM CHLORIDE, POTASSIUM HYDROXIDE?
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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 30KYC7MIAI
Aspartic acid is an amino acid used in pharmaceutical formulations as a pH buffer and to help stabilize active ingredients. It works to maintain the proper acidity level in the medicine.
-
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 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 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII X66NSO3N35
Thiamine is a B vitamin used in some formulations as a nutritional fortification ingredient. It has no technical role in the medicine's structure or stability.
-
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.
6 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesAspartic acid, benzalkonium chloride, glycerin, propylene glycol, purified water, thiamine. Comments, Questions or Complaints? In the U.S. call 833-604-7128, 9:00am - 5:00pm Eastern Standard Time, Monday - Friday, except U.S. holidays or visit www.mdfarma.com available 24 hours.
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 |
|---|---|---|---|---|---|---|
| MDFARMA COLD and FLU RELIEF 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 5 [hp_X]/.2mL; 7 [hp_X]/.2mLthis 73002-0713-03 | Green | 5 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
🏛️
2020
On the market since
Sep 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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 73002-0713-03 You're viewing this | 5 mL in 1 BOTTLE, SPRAY (73002-713-03) | 2020-09-23 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
Marketed without an FDA application
Listed without an FDA application
This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.
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 Drug Other". 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 73002-713-03, 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: 73002-0713-03, written without dashes as 73002071303. 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 73002-0713-03, the first segment (73002) is the labeler code FDA assigned to Green Earth Health Inc.; the middle segment (0713) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 it is currently marketed — but Green Earth Health Inc. has reported a marketing end date of 2026-09-30, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
Green Earth Health 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
🎯 Indications and Usage ▾
Use Temporarily relieves symptoms associated with colds and flu.
⏱️ Dosage and Administration ▾
Directions Do not use if tamperproof cover is missing. Press down 2-3 times to prime the pump. Spray once into each nostril Use 2 times per day to relieve discomfort.
⚠️ Warnings ▾
Warnings If symptoms persist or worsen, discontinue use, seek medical attention. • Avoid contact with eyes. If product gets into eyes, flush with water, seek medical attention. • If pregnant or breastfeeding ask a health professional before use. • Consult a medical professional if using other medications for known interactions. • The use of this dispenser by more than one person may spread infection.
🧪 Active Ingredient ▾
Active Ingredient Active ingredient Purpose Contains atropine (Atropinum) 5X HPUS …………………………………....... runny nose relief Contains cobra venom preparation (Naja naja) 5X HPUS ………..... pain relief Contains magnesium chloride (Magnesia muriatica) 5X HPUS….... cold remedy Contains potassium hydroxide (Kali causticum) 7X HPUS ………. .... flu remedy Reference: the Homeopathic Pharmacopoeia of the United States (HPUS) Contains 24 doses
🧪 Inactive Ingredients ▾
Inactive ingredients Aspartic acid, benzalkonium chloride, glycerin, propylene glycol, purified water, thiamine. Comments, Questions or Complaints? In the U.S. call 833-604-7128, 9:00am - 5:00pm Eastern Standard Time, Monday - Friday, except U.S. holidays or visit www.mdfarma.com available 24 hours.
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.