Rapidol Ointment
FDA Label NDC 55758-440

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pharmadel Llc for the product Rapidol (NDC 55758-440). 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 otc - purpose, uses, warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

Active ingredients Purpose
Bacitracin zinc 400 units ..................First aid antibiotic
Neomycin sulfate 3.5 mg..................First aid antibiotic
Polymyxin B sulfate 5,000 units .......First aid antibiotic

Warnings

For external use only.

Keep Out Of Reach Of Children.

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

Directions

  • clean the affected area
  • apply a small amount of this product (an amount equal to the surface of the tip of a finger) on the area 1 to 3 times daily
  • may be covered with a sterile bandage

Inactive Ingredients

cocoa butter, cottonseed oil, mineral oil, olive oil, paraffin, sodium pyruvate, tocopherol acetate (vit. E), white petrolatum

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