NDC 73002-221 Pain Relief Snake Venom And Hemp

Cobra Venom (naja Naja) 5x, Hemp Extract (cannabis Sativa) 2x, Moccasin Venom (a.piscivorus) 7x

NDC Product Code 73002-221

NDC CODE: 73002-221

Proprietary Name: Pain Relief Snake Venom And Hemp What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Cobra Venom (naja Naja) 5x, Hemp Extract (cannabis Sativa) 2x, Moccasin Venom (a.piscivorus) 7x What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73002 - Green Earth Health Inc.

NDC 73002-221-01

Package Description: 28 mL in 1 BOTTLE, SPRAY

NDC Product Information

Pain Relief Snake Venom And Hemp with NDC 73002-221 is a a human over the counter drug product labeled by Green Earth Health Inc.. The generic name of Pain Relief Snake Venom And Hemp is cobra venom (naja naja) 5x, hemp extract (cannabis sativa) 2x, moccasin venom (a.piscivorus) 7x. The product's dosage form is spray and is administered via oral form.

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.

Pain Relief Snake Venom And Hemp 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.

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.

  • TEA LEAF (UNII: GH42T47V24)
  • 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.

  • Oral - Administration to or by way of the mouth.

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 HOMEOPATHIC - 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: 09-01-2020 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Pain Relief Snake Venom And Hemp Product Label Images

Pain Relief Snake Venom And Hemp 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 Ingredients                                                                                  Purpose

Cobra venom (Naja naja) 5X (0.07mg) HPUS                                        AnalgesicHemp extract (Cannabis sativa) 2X (11.3mg) HPUS                              Anti-inflammatoryMoccasin venom (A.piscivorus) 7X (0.0007mg) HPUS                            AnalgesicApproximately 158 sprays per containerReference: the Homeopathic Pharmacopoeia of the United States (HPUS)


Temporarily relieves pain associated with neuropathy, periodic neuralgia, neck & back pain


• Side effects might include headache, nausea, sore throat, allergic rhinitis, gastrointestinal discomfort, itchiness or mild rash.• If symptoms persist or worsen, stop using this product and consult a physician.• 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.• If diagnosed with psychiatric or mood disorder, seek medical advice before use.• Keep out of reach of children.

Directions For Use:

  • Do not use if tamper proof cover is missing.Press down 4 times to prime the pump.Spray 2 times directly into the mouth or under the tongue.Start using 3 times per day. Use as needed thereafter to relieve discomfort.Allow several days for product to take maximum effect.Use within 60 days from opening. Store at 50° to 75°F (10°C to 24°C)

Other Information:

  • Consult medical professional if using other medications for known interactions.Cannabidiol in hemp extract may alter the metabolism of other drugs.

Inactive Ingredients:

Citric acid, flavoring, glycerin, potassium sorbate, purified water, sodium benzoate, vitamin C, xanthan gum.

* Please review the disclaimer below.