NDC 75568-009 Pain Relief Patches

Lidocaine Pain Relief Patch

NDC Product Code 75568-009

NDC CODE: 75568-009

Proprietary Name: Pain Relief Patches 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 Pain Relief Patch 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

  • 75568 - Planet (anhui) Medical Products Co., Ltd

NDC 75568-009-40

Package Description: 40 mg in 1 PATCH

NDC Product Information

Pain Relief Patches with NDC 75568-009 is a a human over the counter drug product labeled by Planet (anhui) Medical Products Co., Ltd. The generic name of Pain Relief Patches is lidocaine pain relief patch. The product's dosage form is patch and is administered via topical form.

Labeler Name: Planet (anhui) Medical Products Co., Ltd

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 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 Patches 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 40 mg/1000mg

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.

  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POVIDONE (UNII: FZ989GH94E)
  • POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • TARTARIC ACID (UNII: W4888I119H)
  • KAOLIN (UNII: 24H4NWX5CO)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
  • SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)

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: Planet (anhui) Medical Products Co., Ltd
Labeler Code: 75568
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: 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: 12-31-2021 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.

Pain Relief Patches Product Label Images

Pain Relief Patches 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

Otc - Active Ingredient

Lidocaine 4%

Otc - Purpose

Topical anesthetic

Dosage & Administration

For temporary relief of pain

Warnings

For external use only

Otc - Do Not Use

  • Do not usemore than 1 patch at a timeon wounds or damaged skinwith a heating padif you are allergic to any ingredients of this product

Otc - When Using

  • Use only as directedavoid contact with the eyes, mucous membranes or rashesdo not bandage tightly

Otc - Stop Use

  • Localized skin reactions, such as rash, itching, redness, pain, swelling and blistering developconditions worsensymptoms persist for more than 7 dayssymptoms clear up and occur again within a few days

Otc - Pregnancy Or Breast Feeding

Ask a health professional before use

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

  • Adults and children 12 years of age and over:clean and dry affected arearemove film from patch and apply to the skinapply 1 patch at a time to affected area, not more than 3 to 4 times dailypatch should not be applied longer than an 8 hour periodChildren under 12 years of age: consult a doctor

Other Safety Information

  • Avoid storing product in direct sunlightProtect product from excessive moisture

Inactive Ingredient

Dihydroxyaluminum Aminoacetate, Glycerol, Kaolin, Methylparaben, Polyacrylic Acid, Propylene Glycol, Propylparaben, PVP, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Tween 80, Water

* Please review the disclaimer below.