Walgreens Boil Pain Relief Ointment
FDA Label NDC 0363-9095

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreens Company for the product Walgreens Boil Pain Relief (NDC 0363-9095). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, uses, warningsfor external use only, do not use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Benzocaine 20% 

Purpose

Pain Reliever 

Uses

  • for the temporary relief of pain and discomfort casued by boils

Warningsfor External Use Only

Do Not Use

  • for more than 3 days 
    • Ask a doctor before use if you have
    • boils on the lips,nose ,cheeks or foreehead. 

When Using This Product

  • avoid contact with eyes 

Stop Use And Ask A Doctor If

  • fevers occur
  • redness around the bolis develops
  • condition worsens or does not improve
  • symptoms persist for mroe thna 3 days 
  • symptoms clear up and occur again within a few days. 

Directions

  • Adults and children 2 years and older; Apply to the affected areas not more than 2 times daily
  • Children under 2 years;ask a doctor

Other Information

Store as controlled room temperature 20-25 C ( 68-77F)

Inactive Ingredients

Beeswax, Camphor, Eucalyptus Oil, Lanolin, Menthol, Paraffin, Petrolatum, Thymol

Principal Display Panel 1 Oz

Walgreens          NDC 0363-9095-28

Boil Pain Relief Ointment 

Benzocaine 20%/ Pain reliever

NET WT 1 OZ (28g)

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