NA-ZONE- sodium chloride lotion

NA-ZONE by

Drug Labeling and Warnings

NA-ZONE by is a Otc medication manufactured, distributed, or labeled by Snuva, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Enter section text here

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)

INGREDIENTS AND APPEARANCE

NA-ZONE 
sodium chloride lotion

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

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

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

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

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	Business Operations
Snuva, Inc.		807310008	manufacture