Label: NALOXONE HYDROCHLORIDE spray

  • NDC Code(s): 70677-1283-1
  • Packager: Strategic Sourcing Services LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated March 25, 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 medications or 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 ...
  • Warning
    When using this product some 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 833-358-6431
  • Package/Label Principal Display Panel
    NDC 70677-1283-1 - COMPARE TO NARCAN® ACTIVE INGREDIENT - Foster & Thrive™ Original Prescription Strength - Naloxone HCl Nasal Spray 4 mg - Emergency Treatment of Opioid Overdose - EASY TO USE - CAN SAVE A ...
  • INGREDIENTS AND APPEARANCE
    Product Information