NASOCALM SALINE RINSE MIX PACKETS (sodium chloride- nacl powder

Nasocalm Saline Rinse Mix Packets by

Drug Labeling and Warnings

Nasocalm Saline Rinse Mix Packets by is a Otc medication manufactured, distributed, or labeled by Virexion Health Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Chloride (NaCl): 4.05 g

Sodium Bicarbonate (NaHCO₃): 0.45 g

PURPOSE

Nasal Irrigation & Congestion Relief

INDICATIONS & USAGE

1.Helps clear nasal passages and sinuses by flushing out allergens, mucus, and irritants.
2.Relieves nasal congestion due to colds, flu, allergies, and sinusitis.

3.Suitable for daily nasal irrigation and post-surgical nasal care.

WARNINGS

Warnings

1. For nasal rinse only. Do not ingest.
2. Use only sterile, distilled, or previously boiled and cooled water to avoid infections

STOP USE

Discontinue use if nasal irritation, nosebleeds, or persistent discomfort occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

1. Prepare the Solution: Mix one packet with 500 mL (16.91 FL OZ) of sterile or previously boiled and cooled water. Stir until fully dissolved.

2. Perform Nasal Rinse: Lean over a sink, tilt your head slightly, and gently squeeze or pour the solution into one nostril while breathing through your mouth. Allow the solution to drain from the other nostril. Repeat on the other side.

3. After Use: Blow your nose gently to remove excess fluid. Wash your irrigation device thoroughly and let it air dry.

4. Children and infants must be used under adult supervision. For children under 5 years old, please follow the advice of a healthcare professional.

STORAGE AND HANDLING

Store in a cool, dry place.
Keep the packets sealed until use.

INACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NASOCALM SALINE RINSE MIX PACKETS 
sodium chloride (nacl) powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85436-005
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	90 mg  in 100 mg
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	10 mg  in 100 mg

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85436-005-01	50 in 1 BOX	03/28/2025
1		4500 mg in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/28/2025

Labeler - Virexion Health Inc. (243333153)

Establishment
Name	Address	ID/FEI	Business Operations
Virexion Health Inc.		243333153	label(85436-005) , manufacture(85436-005)