Active Ingredient (In Each Spray)
Naloxone Hydrochloride 4 mg
The following Structured Product Label (SPL) was submitted to the FDA by Hf Acquisition Co Llc, Dba Healthfirst for the product Narcan Naloxone Hcl (NDC 51662-1642). 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 active ingredient (in each spray), otc - purpose, uses, warnings, directions, inactive ingredient, otc - questions, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Naloxone Hydrochloride 4 mg
Emergency treatment of opioid overdose
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.
For opioid emergencies, call 911. For questions on NARCAN, call 1-844-4NARCAN (1-844-462-7226) or go to WWW.NARCAN.COM.
©2023 Emergent Devices Inc. EMERGENT® and NARCAN® are registered trademarks of Emergent BioSolutions Inc, or its subsidiaries.
Other Information
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store at room temperature or refrigerated, between 2°C to 25°C (36°F to 77°F)
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do not freeze
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avoid excessive heat above 40°C (104°F)
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protect from light
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the product is packaged in individually-sealed blisters.
Do not use if the blister is open or torn, or if the device appears damaged.
benzalkonium chloride, edetate disodium, hydrochloric acid, sodium chloride, water
Call 1-844-4NARCAN (1-844-462-7226) or go to WWW.NARCAN.COM
keep out of reach of children
* Please review the disclaimer below.