NDC 73287-015 Hempvana Maximum Strength Pain Relief Cream - Night

Lidocaine 4%

NDC Product Code 73287-015

NDC CODE: 73287-015

Proprietary Name: Hempvana Maximum Strength Pain Relief Cream - Night 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 4% 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
    • 73287-015 - Hempvana Maximum Strength Pain Relief Cream - Night

NDC 73287-015-01

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

NDC Product Information

Hempvana Maximum Strength Pain Relief Cream - Night with NDC 73287-015 is a a human over the counter drug product labeled by Telebrands Corp. The generic name of Hempvana Maximum Strength Pain Relief Cream - Night is lidocaine 4%. The product's dosage form is cream and is administered via topical form.

Labeler Name: Telebrands Corp

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 Maximum Strength Pain Relief Cream - Night 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 4 g/100g

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.

  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • ALLANTOIN (UNII: 344S277G0Z)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • MELATONIN (UNII: JL5DK93RCL)
  • CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
  • LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • WATER (UNII: 059QF0KO0R)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • COCOA BUTTER (UNII: 512OYT1CRR)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

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: 05-12-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 12-31-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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 Maximum Strength Pain Relief Cream - Night Product Label Images

Hempvana Maximum Strength Pain Relief Cream - Night 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

Lidocaine 4%

Purpose

Lidocaine 4%.......................Topical Analgesic

Uses

Temporary relief of pain

Warnings

For external use only

Other Safety Information

Allergy 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 within 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

  • For Use By Adults OnlyApply generously to affected areaMassage into painful area until thoroughly absorbed into skin.Repeat as necessary, but no more than 4 times daily.

Inactive Ingredients

Water/Aqua/Eau, Propylene Glycol, Ethylhexyl Palmitate, Dimethicone, Stearic Acid, Cannabis Sativa (Hemp) Seed Oil, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Lavandula Angustifolia (Lavender) Oil, Melatonin, Piper Methysticum Root Extract, Anthemis Nobilis Flower Extract, Lavandula Angustifolia (Lavender) Flower Extract, Theobroma Cacao (Cocoa) Seed Butter, Potassium Cetyl Phosphate, Glycerin, Tocopheryl Acetate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Isohexadecane, Ethylhexylglycerin, Hexylene Glycol, Allantoin, Polysorbate 80, Disodium EDTA, Sodium Hydroxide, Red 4 (CI 14700), Blue 1 (CI 42090)

Questions?

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

* Please review the disclaimer below.