OTC Medication Information: NA-ZONE
NA-ZONE — sodium chloride lotion
Snuva, Inc.
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
SODIUM CHLORIDE
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
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 TIMESWARNINGS
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)
NA-ZONE FRONTNA-ZONE BACK
NA-ZONE sodium chloride lotion | |||||||||||||
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Labeler — Snuva, Inc. (807310008) |
Registrant — Snuva, Inc. (807310008) |
Establishment | |||
Name | Address | ID/FEI | Operations |
Snuva, Inc. | 807310008 | manufacture |
Revised: 11/2010 Snuva, Inc.
Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.