NASOCALM (sodium chloride- nacl solution

Nasocalm by

Drug Labeling and Warnings

Nasocalm 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) 0.9%

PURPOSE

Hydrates, soothes, and clears nasal passages, relieves mild congestion, and flushes out allergens, dust, and pollutants, suitable for daily nasal hygiene for all ages.

INDICATIONS & USAGE

1. Gently cleanses the nasal passages and moisturizes nasal tissues.
2. Helps remove allergens, mucus, and airborne pollutants.
3. Suitable for daily nasal hygiene, allergy relief, and post-surgical care.

WARNINGS

For nasal use only. Not for injections.

DO NOT USE

Do not use if the packaging is damaged or the solution appears cloudy.

STOP USE

Stop use and consult a doctor if irritation or infection occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

1. Tilt your head slightly forward

2. Insert the nozzle into one nostril

3. Gently squeeze the bottle to release the solution

4. After application, gently blow your nose if necessary

5. Repeat in the other nostril

6. Use 2-6 times per day or as needed

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

INACTIVE INGREDIENT

Purified water USP

STORAGE AND HANDLING

1. Store at room temperature (15-30°C or 59-86°F).

2. Protect from extreme heat and direct sunlight.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NASOCALM 
sodium chloride (nacl) solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85436-002
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	0.9 mg  in 100 mg

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

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85436-002-01	60 in 1 BOX	03/28/2025
1		5 mg in 1 VIAL; Type 0: Not a Combination Product
2	NDC: 85436-002-02	20 in 1 BOX	03/28/2025
2		15 mg in 1 VIAL; 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	manufacture(85436-002) , label(85436-002)