0.9 PERCENT SALINE SOLUTION- sodium chloride liquid

0.9 percent saline solution by

Drug Labeling and Warnings

0.9 percent saline solution by is a Otc medication manufactured, distributed, or labeled by EMPIRE GROUPS LLC, Guangzhou Jinsheng Biotechnology Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredien: Sodium Chloride 0.9%

INACTIVE INGREDIENT

Inactive ingredien: USP Water

WARNINGS

Warings:

NOT FOR INJECTION;

Only use sealed vials do not use if vialis broken or already open

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:
Do not use after expiration date;
Discontinue if you experience any adverse reaction and call your physician

DOSAGE & ADMINISTRATION

Single use dosage vials 5ml each

INDICATIONS & USAGE

Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler.

If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.

PURPOSE

Uses: Moisturizer

For dry nasal membranes

QUESTIONS

Question:

emipregrp@gmail.com

PRINCIPAL DISPLAY PANEL

See Label

INGREDIENTS AND APPEARANCE

0.9 PERCENT SALINE SOLUTION 
sodium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85602-101
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85602-101-02	30 in 1 BOX	04/30/2025
1	NDC: 85602-101-01	5 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
unapproved drug other		04/30/2025

Labeler - EMPIRE GROUPS LLC (126061466)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Jinsheng Biotechnology Corporation		402822781	manufacture(85602-101)