Label: NALOXONE HYDROCHLORIDE spray

  • NDC Code(s): 68001-645-45
  • Packager: BluePoint Laboratories
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 17, 2025

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  • Active Ingredient (in each spray)
    Naloxone hydrochloride 4 mg
  • Purpose
    Emergency treatment of opioid overdose
  • Uses
    •to “revive” someone during an overdose from many - prescription pain medicationsor - street drugs such as heroin - •this medicine can save a life
  • Directions
    Emergency Treatment of Opioid Overdose - Important: For use in the nose only - Do not test nasal spray device before use - 1 nasal spray device contains 1 dose of medicine - Each device ...
  • Warning
    When using this productsome people may experience symptoms when they wake up, such as shaking, sweating, nausea, or feeling angry. This is to be expected
  • Other information
    •store at room temperature or refrigerated, between 2°C to 25°C (36°F to 77°F) •do not freeze - •avoid excessive heat above 40°C (104°F) •protect from light - •the product is packaged in ...
  • Inactive Ingredients
    benzalkonium chloride, edetate disodium, hydrochloric acid, sodium chloride, water
  • Questions?
    call 1-866-634-9120 or go to www.padagis.com
  • Package/Label Principal Display Panel
    NDC 68001-645-45 - Naloxone HCl Nasal Spray 4 mg - Emergency Treatment of Opioid Overdose - Original Prescription Strength - Easy to Use - Can Save a Life - Designed to Rapidly Reverse the Effects of a ...
  • INGREDIENTS AND APPEARANCE
    Product Information