NDC 72137-223 Cbd-kings With Lidocaine 4%

Lidocaine, Menthol, Methyl Salicylate, Camphor

NDC Product Code 72137-223

NDC Code: 72137-223

Proprietary Name: Cbd-kings With Lidocaine 4% Additional informationCallout TooltipWhat 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, Menthol, Methyl Salicylate, Camphor Additional informationCallout TooltipWhat 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.


Code Structure
  • 72137 - 1st Medx Llc
    • 72137-223 - Cbd-kings

NDC 72137-223-05

Package Description: 5 PATCH in 1 POUCH > 1 PATCH in 1 PATCH

NDC Product Information

Cbd-kings With Lidocaine 4% with NDC 72137-223 is a a human over the counter drug product labeled by 1st Medx Llc. The generic name of Cbd-kings With Lidocaine 4% is lidocaine, menthol, methyl salicylate, camphor. The product's dosage form is patch and is administered via topical form.

Labeler Name: 1st Medx Llc

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Cbd-kings With Lidocaine 4% Active Ingredient(s)

Additional informationCallout TooltipWhat 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 1/1
  • MENTHOL 3 1/1
  • METHYL SALICYLATE 9 1/1
  • CAMPHOR OIL 1.2 1/1

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • HEMP (UNII: TD1MUT01Q7)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
  • DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • TARTARIC ACID (UNII: W4888I119H)
  • SORBITOL (UNII: 506T60A25R)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: 1st Medx Llc
Labeler Code: 72137
FDA Application Number: part348 Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 01-31-2019 Additional informationCallout TooltipWhat 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: 12-31-2020 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Cbd-kings With Lidocaine 4% Product Label Images

Cbd-kings With Lidocaine 4% 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:

LIDOCAINE 4%MENTHOL 3%METHYL SALICYLATE 9%CAMPHOR 1.2%

Purpose

TOPICAL ANESTHETICTOPICAL ANALGESICTOPICAL ANALGESICTOPICAL ANALGESIC

Uses:

FOR THE TEMPORARY RELIEF OF MINOR ACHES AND PAINS OF MUSCLES AND JOINTS ASSOCIATED WITH ARTHRITIS, SIMPLE BACKACHE, STRAINS, SPRAINS, MUSCLE SORENESS AND STIFFNESS.

Warnings:

  • FOR EXTERNAL USE ONLY.USE ONLY AS DIRECTED.AVOID CONTACT WITH EYES AND MUCOUS MEMBRANES.DO NOT USE ON WOUNDS, CUTS, DAMAGED OR INFECTED SKIN AS WELL AS IN THE EYES, MOUTH, GENITALS, OR ANY OTHER MUCOUS MEMBRANES.DO NOT COVER WITH BANDAGES.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.IF SWALLOWED, CALL POISON CONTROL

Warnings And Precautions

  • IF CONTACT DOES OCCUR WITH EYES, RINSE WITH COLD WATER AND CALL A DOCTOR.CHILDREN UNDER 12 YEARS OLD, CONSULT A DOCTOR BEFORE USE.IF YOU ARE ALLERGIC TO ANY INGREDIENTS IN THIS PRODUCT CONSULT A DOCTOR BEFORE USE.CONSULT YOUR PHYSICIAN: IF PREGNANT OR IF PAIN PERSISTS OR WORSENS.

Directions:

FOR ADULTS AND CHILDREN 12 YEARS AND OVER. APPLY PATCH TO AFFECTED AREA 1 TO 2 TIMES DAILY OR AS DIRECTED BY PHYSICIAN. CLEAN AND DRY THE AFFECTED AREA. OPEN POUCH AND REMOVE PROTECTIVE FILM AND APPLY PATCH TO AFFECTED AREA. WASH HANDS WITH SOAP AND WATER AFTER APPLYING PATCH. RESEAL POUCH CONTAINING UNUSED PATCHES AFTER USE.

Other Information:

STORE BELOW 90°F/32°C

Inactive Ingredients:

HEMP OIL 125MG, GLYCERIN 25%, POLYACRYLIC ACID 5%, PROPYLENE GLYCOL 2%, METHYL SALICYLATE, GLYCERIN, SODIUM POLYACRYLATE, DIHYDROXYALUMINUM AMINOACETATE, ISOPROPYL MYRISTATE, TARTARIC ACID, PROPYLENE GLYCOL, SORBITOL, EDTA2-NA, PROPYL  P-HYDROXYBENZOATE, TWEEN 80, TITANIUM DIOXIDE, EXTRA MEDICAL PURIFIED WATER.

Questions?

888-319-6339

* Please review the disclaimer below.

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