GURUNANDA NASAL SALINE- nasal wash powder, for solution

GURUNANDA NASAL SALINE by

Drug Labeling and Warnings

GURUNANDA NASAL SALINE by is a Otc medication manufactured, distributed, or labeled by GURUNANDA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Sodium Bicarbonate USP 515mg

Sodium Chloride USP 1685 mg

Purpose

Nasal Wash

Uses

• Restores vital moisture to provide prompt relief for dry , crusted and inflamed nasal membranes due to chronic sinusitis,colds , low humidity, overuse of nasal decongestant drops and sprays, allergies, minor nose bleeds and other minor nasal irritations.
• Temporarily relieves nasal stuffiness.
• Reduces swelling of nasal passages; shrinks swollen membranes.
• Promotes nasal and/or sinus drainage; temporarily relieves sinus congestion and pressure.

Warnings

• Do not exceed recommended dosage.
• This product may cause temporary discomfort such as burning , stinging, sneezing or an increase in nasal discharge.
• The use of this container by more than one person may spread infection.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

• Adults and children 4 years and over: Use 1-2 packets per 240 ml upto to every 2 hours as needed
• Children under 4 years : Consult a Physician

Other Information

• Inspect saline packets for integrity
• Do not use saline packets if open or torn
• Protect saline packets from excessive heat and moisture
• See saline packets oe box for lot# and expiration date

Inactive Ingredients

None

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GURUNANDA NASAL SALINE 
nasal wash powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70708-210
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	0.515 g  in 2.2 g
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	1.685 g  in 2.2 g

Product Characteristics
Color	white (WHITE CRYSTALLINE GRANULE POWDER)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70708-210-08	8 in 1 BOX	02/12/2024
1		2.2 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/12/2024

Labeler - GURUNANDA LLC (079671169)