Saline by Healthlife of USA / Kingston Pharma LLC SALINE spray

Saline by

Drug Labeling and Warnings

Saline by is a Otc medication manufactured, distributed, or labeled by Healthlife of USA, Kingston Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Sodium Chloride 0.65%

Purpose 

For allergies: cold, flu, sinusitis, rhinitis and dry irritated nasal passages

Ingredients 

A solution of sodium chloride 0.65% in purified water (USP), made isotonic with sodium phosphate dibasic and sodium phosphate monobasic, with benzyl alcohol and benzalkonium chloride as preservatives.

Uses

for dry nasal membranes squeeze twice in each nostril as needed.

Directions

upright delivers as a spray, horizontally as a stream, upside down as a drop.

Warnings

If pregnant or breast-feeding, ask a healthcare professional before use. Use of this container by more than one person may spread infection.

Keep out of reach  of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Questions or comments?

Call 1-844-832-1138

*This product is not manufactured or distributed by Valeant Consumer Products, Distributors of Ocean Saline Nasal Spray.

Saline Nasal Spray 

Distributed by:

Healthlife of USA

1600 Hart Street,

Rahway, NJ 07065

www.healthlifeofusa.com

INGREDIENTS AND APPEARANCE

SALINE 
saline spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69517-609
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69517-609-19	1 in 1 CARTON	01/10/2018
1		44 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/10/2018

Labeler - Healthlife of USA (079656178)

Establishment
Name	Address	ID/FEI	Business Operations
Kingston Pharma LLC		080386521	manufacture(69517-609)