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.

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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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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
sodium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58291-0011
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	.65 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:58291-0011-1	59 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	01/01/1989

Labeler - Snuva, Inc. (807310008)

Registrant - Snuva, Inc. (807310008)

Name	Address	ID/FEI	Business Operations
Establishment
Snuva, Inc.		807310008	manufacture