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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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Active Ingredient (in each spray) Naloxone hydrochloride 4 mg
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Purpose Emergency treatment of opioid overdose
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Uses • to “revive” someone during an overdose from many prescription pain medications or street drugs such as heroin - • this medicine can save a life
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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 ...
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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.
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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 ...
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Inactive Ingredients benzalkonium chloride, edetate disodium, hydrochloric acid, sodium chloride, water
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Questions? call 833-358-6431
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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 ...
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INGREDIENTS AND APPEARANCEProduct Information