NDC 0363-4012 Walgreens Pain Relieving

NDC Product Code 0363-4012

NDC CODE: 0363-4012

Proprietary Name: Walgreens Pain Relieving 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.

NDC Code Structure

NDC 0363-4012-19

Package Description: 453 g in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Walgreens Pain Relieving with NDC 0363-4012 is a product labeled by Walgreen Co.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1361205.

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.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Walgreen Co.
Labeler Code: 0363
Start Marketing Date: 08-07-2013 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Walgreens Pain Relieving Product Label Images

Walgreens Pain Relieving 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 0.7%Menthol  0.2%


External AnalgesicExternal Analgesic


  • Temporary relief of pain and itchinghelps relieve and soothes pain from sunburn, minor burns, cuts, scrapes, skin irritations and insect bites.


For external use onlyDo not use in large quantities, particularly over raw surfaces or blistered areas.

When Using This Product

  • Avoid contact with eyes.

Stop Use And Ask A Doctor If

  • Conditions worsens or if symptoms persists for more than 7 days.symptoms clear up and occur again within a few days.

Keep Out Of The Reach Of Children.

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


  • Adults and children 2 years of age and older.apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: do not use, ask a doctor.

Inactive Ingredients

Water, Alcohol Denat., Glycerin, Polysorbate 20, Carbomer, Aloe Barbadensis Leaf Juice, Benzophenone-4, Tocopherol, Imidazolidinyl Urea, Blue 1.

* Please review the disclaimer below.