Drug Facts Active Ingredients
Sodium Chloride .9%
Nebuclear Md Saline Liquid
FDA Label NDC 73117-522
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Echo Care Llc for the product Nebuclear Md Saline (NDC 73117-522). 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 drug facts active ingredients, purpose, uses, warnings, storage, keep out of reach of children, direction, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Moisturizer
Uses
Moisturizing dry nasal passages and relieves nasal dryness associated with colds, allergies, sinusitis or dry air.
Warnings
Not for Injection
Do not use after expiration date
Discontinue if you experience any adverse reactions and call your physician
Only use sealed vials
Do not use if vial is broken
Storage
Store at room temperature
Avoid freezing or excessive heat
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222
Direction
Adults and children: Administer into nasal passageway as often as needed or as directed by a physician. For infants, apply using drops. Follow the instructions provided with the delivery device for proper administration. To help prevent the spread of infection, do not share the dispenser or delivery device with others.
Inactive Ingredient
Water
Questions Or Comments
Package Label.Principal Display Panel
Contains 100 NebuClear MD® Saline 5mL vials
* Please review the disclaimer below.
