NDC 66902-257 Cvs Lidocaine Pain Relief Dry

Menthol, Unspecified Form, Lidocaine

NDC Product Code 66902-257

NDC CODE: 66902-257

Proprietary Name: Cvs Lidocaine Pain Relief Dry 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, Unspecified Form, Lidocaine 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

  • 66902 - Natural Essentials, Inc.

NDC 66902-257-04

Package Description: 113 g in 1 CAN

NDC Product Information

Cvs Lidocaine Pain Relief Dry with NDC 66902-257 is a a human over the counter drug product labeled by Natural Essentials, Inc.. The generic name of Cvs Lidocaine Pain Relief Dry is menthol, unspecified form, lidocaine. The product's dosage form is spray and is administered via topical form.

Labeler Name: Natural Essentials, Inc.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Cvs Lidocaine Pain Relief Dry 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.

  • MENTHOL, UNSPECIFIED FORM 10 mg/g
  • LIDOCAINE 40 mg/g

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • 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: Natural Essentials, Inc.
Labeler Code: 66902
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: 01-21-2021 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 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.

Cvs Lidocaine Pain Relief Dry Product Label Images

Cvs Lidocaine Pain Relief Dry 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 1%

Purpose

Topical analgesic
Topical analgesic

Use

  • Temporarily relieves minor pain

Warnings

  • For external use onlyFlammable:do not use while smoking or near heat or flame
  • Avoid long term storage above 104°F (40°C)
  • Do not store at temperatures above 120°F (49°C)

Do Not Use

  • On large areas of the body
  • On cut, damaged, irritated or swollen skin
  • More than one week without consulting a doctor

When Using This Product

  • Use only as directed
  • Rare cases of serious burns have been reported with products of this type
  • Do not allow contact with eyes or mucous membranes
  • Avoid spraying on face
  • Avoid inhalation of spray
  • Do not bandage tightly
  • Do not use with a heating pad or other topical pain relief products
  • Contents under pressure
  • Do not puncture or incinerate.

Stop Use And Ask A Doctor If

  • Condition worsens
  • Redness is present
  • Irritation develops
  • Symptoms persist for more than 7 days or clear up and occur again within a few days
  • Needed for longer than a week

If Pregnant Or Breast-Feeding,

  • Ask a health professional before use.

Keep Out Of Reach Of Children And Pets.

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

Directions

  • Shake well
  • Adults and children 12 years of age and older:spray product on area not more than 1 to 3 times daily
  • Product will dry quickly on its own, and does not need to be rubbed in
  • Children under 12 years of age or younger: ask a doctor

Inactive Ingredients

Alcohol Denatured, Caprylic/Capric Triglyceride, Propylene Glycol

* Please review the disclaimer below.