NDC 73615-103 Md Science Cannabidiol

Lidocaine And Histamine Dihydrochloride

NDC Product Code 73615-103

NDC CODE: 73615-103

Proprietary Name: Md Science Cannabidiol 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: Lidocaine And Histamine Dihydrochloride 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to relieve nerve pain after shingles (infection with the herpes zoster virus). This type of pain is called post-herpetic neuralgia. Lidocaine helps to reduce sharp/burning/aching pain as well as discomfort caused by skin areas that are overly sensitive to touch. Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.

NDC Code Structure

  • 73615 - Md Natural Health Llc

NDC 73615-103-03

Package Description: 1 BOTTLE, PLASTIC in 1 BOX > 88 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Md Science Cannabidiol with NDC 73615-103 is a a human over the counter drug product labeled by Md Natural Health Llc. The generic name of Md Science Cannabidiol is lidocaine and histamine dihydrochloride. The product's dosage form is cream and is administered via topical form.

Labeler Name: Md Natural Health Llc

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Md Science Cannabidiol 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.

  • LIDOCAINE 37.8 mg/mL

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.

  • EMU OIL (UNII: 344821WD61)
  • SORBITOL (UNII: 506T60A25R)
  • STEARETH-21 (UNII: 53J3F32P58)

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Md Natural Health Llc
Labeler Code: 73615
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 02-15-2020 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’.

* Please review the disclaimer below.

Md Science Cannabidiol Product Label Images

Md Science Cannabidiol 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


Drug Facts

  • Avoid contact with eyes.For external use only.

Distributed By: MD Natural Health 2590 N. Powerline Rd Pompano Beach Florida 33069

Otc - Purpose

Active IngredientsPurpose  Lidocaine 4%AnalgesicHistamine Dihydrochloride 0.08%Counterirritant


Helps in temporary pain relief


  • If this product, used as directed, does not provide relief, discontinue use and consult a doctor.For topical use only.Do not bandage tightly

Otc - Do Not Use

  • Do not use if you are allergic to Lidocaine or topical anesthetics.

  • Do not use on broken, irritated or sensitive skin.

Otc - Stop Use

  • Discontinue use if you develop a rash or irritation, such as burning or itching.

Otc - Ask Doctor

  • If symptoms persist, consult a doctor.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center.


Apply desired amount directly to the area to be affected.

Other Information

STORE AT 20-25° C (68-77° F)

Inactive Ingredients

Aloe Barbadensis (Aloe)Leaf Juice, Caprylhydroxamic Acid, Caprylyl Glycol, Carbomer, CBD (Cannabidiol), Cetyl Esters, Cocos Nucifera (Coconut) Oil, Emu Oil, Glycerin, Glyceryl Stearate, Isopropyl Palmitate, Methylsulfonylmethane (MSM), Sodium Hydroxide, Sorbitol, Steareth-21, Stearyl Alcohol, Water.

* Please review the disclaimer below.