Naloxone Hydrochloride Spray
FDA Label NDC 72162-2376

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bryant Ranch Prepack for the product Naloxone Hydrochloride (NDC 72162-2376). 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), purpose, uses, directions, warning, other information, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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 device sprays 1 time only
  • Do not test nasal spray device before use

    1 nasal spray device contains 1 dose of medicine

    Each device sprays 1 time only

Holding Nasal Spray Device (Device)

Holding Nasal Spray Device (Device)

Step 1 (Step1)

Step 1 (Step1)

Step 1: CHECK if you suspect an overdose:

CHECK for a suspected overdose: the person will not wake up or is very sleepy or not breathing well

yell “Wake up!”

shake the person gently

if the person is not awake, go to Step 2

Step 2 (Step2)

Step 2 (Step2)

Step 2: GIVE 1st dose in the nose

HOLD the nasal spray device with your thumb on the bottom of the plunger

INSERT the nozzle into either NOSTRIL

PRESS the plunger firmly to give the 1st dose

1 nasal spray device contains 1 dose

Step 3 (Step3)

Step 3 (Step3)

Step 3: CALL

CALL 911immediately after giving the 1st dose

Step 4 (Step4)

Step 4 (Step4)

Step 4: WATCH & GIVE

WAIT2-3 minutes after the 1st dose to give the medicine time to work

if the person wakes up: Go to Step 5

if the person does not wake up:

   • CONTINUE TO GIVE doses every 2-3 minutes until the person wakes up

it is safe to keep giving doses

Step 5 (Step5)

Step 5 (Step5)

Step 5: STAY

STAY until ambulance arrives: even if the person wakes up

GIVE another dose if the person becomes very sleepy again

You may need to give all the doses in the pack

For opioid emergencies, call 911. For questions on Naloxone HCl Nasal Spray 4 mg, call Padagis® at 1-866-634-9120 or go to www.padagis.com.

64Q00 RT QS2

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 individually-sealed blisters.

   Do not use if the blister is open or torn, or if the device appears damaged

Inactive Ingredients

benzalkonium chloride, edetate disodium, hydrochloric acid, sodium chloride, water

Questions?

  • call 1-866-634-9120 or go to www.padagis.com

How Supplied

Naloxone HCl Nasal Spray 4 mg

NDC: 72162-2376-2: 2 Single-Dose Vials in a Carton

Store at room temperature or refrigerated, between 2°C to 25°C (36°F to 77°F)

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Package Label.Principal Display Panel

Naloxone HCl 4mg Nasal Spray #2

Label (Lbl721622376)

Label (Lbl721622376)

* Please review the disclaimer below.