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 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 SPRAY
MANUFACTURED FOR SNUVA INC 715 SOUTH BLVD OAK PARK IL 2 FL OZ (59 ml)
NA-ZONE FRONT
(click image for full-size original)

NA-ZONE BACK
(click image for full-size original)

NA-ZONE FRONTNA-ZONE BACK
NA-ZONE
sodium chloride lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:58291-0011
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE (SODIUM CATION) SODIUM CHLORIDE .65 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
EDETATE DISODIUM
BENZALKONIUM CHLORIDE
SODIUM BICARBONATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58291-0011-1 59 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part349 01/01/1989
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.

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.

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