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NA-ZONE

Medically reviewed on November 23, 2017

Dosage form: lotion
Ingredients: SODIUM CHLORIDE .65mL in 100mL
Labeler: Snuva, Inc.
NDC Code: 58291-0011

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.

ACTIVE INGREDIENT

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

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DIRECTIONSDIRECTIONS - 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 LABELNA-ZONE STERILE SALINE NASAL SPRAY
MANUFACTURED FOR SNUVA INC 715 SOUTH BLVD OAK PARK IL 2 FL OZ (59 ml)



NA-ZONE 
sodium chloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58291-0011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (SODIUM CATION) SODIUM CHLORIDE.65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
EDETATE DISODIUM 
BENZALKONIUM CHLORIDE 
SODIUM BICARBONATE 
Packaging
#Item CodePackage Description
1NDC:58291-0011-159 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/1989
Labeler - Snuva, Inc. (807310008)
Registrant - Snuva, Inc. (807310008)
Establishment
NameAddressID/FEIOperations
Snuva, Inc.807310008manufacture

 
Snuva, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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