NDC 0363-9226 First Aid Burn

Lidocaine

NDC Product Code 0363-9226

NDC CODE: 0363-9226

Proprietary Name: First Aid Burn 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 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 product is used to help reduce itching and pain from certain skin conditions (such as scrapes, minor skin irritations, insect bites). It may also be used to help relieve nerve pain after shingles (infection with herpes zoster virus). 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

  • 0363 - Walgreen Company

NDC 0363-9226-06

Package Description: 170 g in 1 CAN

NDC Product Information

First Aid Burn with NDC 0363-9226 is a a human over the counter drug product labeled by Walgreen Company. The generic name of First Aid Burn is lidocaine. The product's dosage form is spray and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1442274.

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.

First Aid Burn 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.

  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
  • SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • WATER (UNII: 059QF0KO0R)
  • EDETIC ACID (UNII: 9G34HU7RV0)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)

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: Walgreen Company
Labeler Code: 0363
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: 01-15-2019 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 - 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.

First Aid Burn 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 0.5%

Purpose

External analgesic

Use

INDICATIONS & USAGE SECTIONTemporarily relieves pain and itching due to:

• Sunburn • Minor burns

• Minor cuts • Scrapes

• Insect bites • Minor skin irritations

Dosage & Administration

For the temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, and poison oak.

Warnings

For external use only.Flammable: Do not spray while smoking or near heat or flame.

Do Not Use

Do not use in large quantities, particularly over raw surfaces or

blistered areas.

When Using This Product:

When using this product:

• Keep out of eyes.

• Use only as directed.

• Do not puncture or incinerate. Contents under pressure. Do

not store at temperature above 120°F.

Stop Use And Ask A Doctor If:

Stop use and ask a doctor if:

• Condition gets worse

• Symptoms last more than 7 days

• Symptoms clear up and occur again in a few days

Keep Out Of Reach Of Children.

Keep out of reach of children. If swallowed, get medical help or

contact Poison Control Center right away.

Directions

• Shake well

• 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: ask a doctor

• To apply to face, spray on palm of hand and gently apply

Inactive Ingredients

Water, Glycerin, Propanediol, Aloe Barbadensis Leaf Juice,

Carbomer, Tocopheryl Acetate, PEG-40 Hydrogenated Castor Oil,

Sodium Lauroyl Sarcosinate, Disodium EDTA, Phenoxyethanol,

Sodium Hydroxide

* Please review the disclaimer below.