Active Ingredient
SODIUM CHLORIDE
Na-zone
FDA Label NDC 58291-0011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Snuva, Inc. for the product Na-zone (NDC 58291-0011). 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 active ingredient, inactive ingredients, purpose, use, keep out of reach of children, directions, warnings, na-zone label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
BENZALKONIUM CHLORIDE
DISODIUM EDTA
DEIONIZED WATER
SODIUM BICARBONATE
Purpose
STERILE SALINE NASAL SPRAY
Use
SAFETY TO USE AS OFTEN AS NEEDED
Keep Out Of Reach Of Children
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Directions
DIRECTIONS - WITH BOTTLE UPRIGHT SQUEEZE FIRMLY AND QUICKLY TO ATOMIZE NA-ZONE INTO EACH NOSTRIL. RELEASE BOTTLE TO VENT AND REPEAT 2 OR 3 TIMES
Warnings
STERILITY GUARANTEED UNTIL THE SEAL IS BROKEN. NO SIDE EFFECTS ONCE SEAL IS BROKEN USE BY ONLY ONE PERSON IS RECOMMENDED
Na-Zone Label
NA-ZONE STERILE SALINE NASAL SPRAYMANUFACTURED FOR SNUVA INC 715 SOUTH BLVD OAK PARK IL 2 FL OZ (59 ml)
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