NDC 73287-019 Hempvana Ultra Strength Pain Relief Cream - Deep Freeze

Menthol

NDC Product Code 73287-019

NDC CODE: 73287-019

Proprietary Name: Hempvana Ultra Strength Pain Relief Cream - Deep Freeze 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: Menthol 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

  • 73287 - Telebrands Corp
    • 73287-019 - Hempvana Ultra Strength Pain Relief Cream - Deep Freeze

NDC 73287-019-01

Package Description: 1 JAR in 1 CARTON > 119 g in 1 JAR

NDC Product Information

Hempvana Ultra Strength Pain Relief Cream - Deep Freeze with NDC 73287-019 is a a human over the counter drug product labeled by Telebrands Corp. The generic name of Hempvana Ultra Strength Pain Relief Cream - Deep Freeze is menthol. The product's dosage form is cream and is administered via topical form.

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.

Hempvana Ultra Strength Pain Relief Cream - Deep Freeze 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.

  • PEG-100 STEARATE (UNII: YD01N1999R)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • VITIS VINIFERA SEED (UNII: C34U15ICXA)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • WATER (UNII: 059QF0KO0R)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

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.

Product Labeler Information

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

Labeler Name: Telebrands Corp
Labeler Code: 73287
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: 10-29-2021 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.

Hempvana Ultra Strength Pain Relief Cream - Deep Freeze 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

Menthol 10%

Purpose

Menthol 10%...................Topical Analgesic

Uses

  • Temporarily relieves minor pain associated with:arthritissimple backachemuscle strainssprainsbruises

Warnings

For external use onlyAllergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Otc - When Using

  • When using this productuse only as directed. Read and follow all directions and warnings on this label.do not bandage tightly or apply local heat (such as heating pads) to the area of use.avoid contact with eyes or mucous membranes.do not apply to wounds or damaged, broken or irritated skin.do not use at the same time as other topical analgesics.

Otc - Stop Use

  • Stop use and ask a doctor ifcondition worsenssymptoms persist for more than 7 days or clear up and occur again wthin a few daysredness is present or irritation develops

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: consult a physician.

Inactive Ingredients

Water/Aqua/Eau, Caprylic/Capric Triglyceride, Glyceryl Stearate, Glycerin, Dimethicone, Cetearyl Alcohol, Cannabis Sativa (Hemp) Seed Oil, PEG-100 Stearate, Stearic Acid, Potassium Cetyl Phosphate, Ilex Paraguariensis Leaf Extract, Vitis Vinifera (Grape) Seed Oil, Tocopheryl Acetate, Phenoxyethanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ethylhexylglycerin, Sodium Hydroxide, Disodium EDTA, Blue 1 (CI 42090)

Questions?

Questions? Call (855) 877-4503 (M-F, 9am-5pm EST)

* Please review the disclaimer below.