Otc - Active Ingredient
.9% Sodium Chloride
Nebuclear Md Liquid
FDA Label NDC 73117-520
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 (NDC 73117-520). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, directions, other safety information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Saline for Inhalation
Indications & Usage
For moistening of the nasal, throat and lungs
Warnings
see a doctor if you:
- Get worse
- Need more than 12 inhalations in 24 hours
- Use more than 9 inhalations in 24 hours for 3 or more days a week
- Ever been hospitalized for asthma
- Heart disease
- High blood pressure
- Diabetes
- Thyroid disease
- Seizures
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- Do not use more than directed
- For use with a Nebulizer.
- Add 0.5 mL (contents of one vial) of solution to Nebulizer.
Other Safety Information
Protect from light. Avoid excessive heat. Protect from freezing.
Store between 2°C and 25°C (36°F and 77°F).
How Supplied: NebuClear MD® Saline Solution, .9$ Sodium Chloride, 5mL vials
20 vials
Inactive Ingredient
water
Otc - Questions
1 (855) 860-3404
Monday through Friday, 8:00 a.m. to 5:00 p.m. (Pacific Standard Time).
Manufactured By:
Blue Echo Care LLC
3639 SE 21st Ave
Portland, OR 97202 USA
Package Label.Principal Display Panel
Contains 20 NebuClear MD® Saline vials
* Please review the disclaimer below.
