NDC 73002-713 Mdfarma Cold And Flu Relief

Atropine, Naja Naja Venom, Magnesium Chloride, Potassium Hydroxide

NDC Product Information

Mdfarma Cold And Flu Relief with NDC 73002-713 is a a human over the counter drug product labeled by Green Earth Health Inc.. The generic name of Mdfarma Cold And Flu Relief is atropine, naja naja venom, magnesium chloride, potassium hydroxide. The product's dosage form is spray and is administered via nasal form.

Labeler Name: Green Earth Health Inc.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Mdfarma Cold And Flu Relief Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ATROPINE 5 [hp_X]/.2mL
  • NAJA NAJA VENOM 5 [hp_X]/.2mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Nasal - Administration to the nose; administered by way of the nose.
  • Nasal - Administration to the nose; administered by way of the nose.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Green Earth Health Inc.
Labeler Code: 73002
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-23-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Mdfarma Cold And Flu Relief Product Label Images

Mdfarma Cold And Flu Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Active ingredient                                                                       PurposeContains atropine (Atropinum) 5X HPUS ………………………………….......  runny nose reliefContains cobra venom preparation (Naja naja) 5X HPUS ……….....  pain reliefContains magnesium chloride (Magnesia muriatica) 5X HPUS…....  cold remedyContains potassium hydroxide (Kali causticum) 7X HPUS ………. .... flu remedyReference: the Homeopathic Pharmacopoeia of the United States (HPUS) Contains 24 doses


Temporarily relieves symptoms associated with colds and flu.


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.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


  • Do not use if tamperproof cover is missing.Press down 2-3 times to prime the pump.Spray once into each nostrilUse 2 times per day to relieve discomfort.

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.

* Please review the disclaimer below.