NEBUCLEAR MD- saline liquid

NebuClear MD by

Drug Labeling and Warnings

NebuClear MD by is a Otc medication manufactured, distributed, or labeled by Blue Echo Care LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

.9% Sodium Chloride

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

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

QUESTIONS

1 (855) 860-3404

support@blueechocare.com

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

PRINCIPAL DISPLAY PANEL

Contains 20 NebuClear MD® Saline vials

INGREDIENTS AND APPEARANCE

NEBUCLEAR MD 
saline liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73117-520
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	9 mg  in 9 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73117-520-19	20 mg in 1 BOX; Type 0: Not a Combination Product	09/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	09/01/2025

Labeler - Blue Echo Care LLC (117048847)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Echo Care LLC		117048847	manufacture(73117-520)