0.9 PERCENTSALINE- sodium chloride solution

0.9 percentsaline by

Drug Labeling and Warnings

0.9 percentsaline by is a Otc medication manufactured, distributed, or labeled by Huizhou Jinsheng Medical Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Cleaning solution

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Straighten the cleaning solution Pour it into the cleaning position for cleaning

Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.

WARNINGS

NOT FOR INJECTION

Only use sealed vials do not use if vial is broken or already open

Do not use After expiration date

Discontinue if you experience any adverse reaction and call your physician

Not for injection, for extemal use only

Do not use if allergicto any of stated Ingredients,if irritation occurs, discon tinue use and consult your doctor or speclalist

Do not heat liqud

Do not use after erplry date

Do not use unless seals Intact before use

DOSAGE & ADMINISTRATION

Single use dosage vials 15ml each

ACTIVE INGREDIENT

Active ingredient: Sodium Chloride 0.9%

INACTIVE INGREDIENT

Inactive ingredient: USP Water

OTHER SAFETY INFORMATION

Other Information:
1. Do not use after expiration date
2. Take care to prevent crushing, sharp objects, moisture and oil contamination during transportation.

QUESTIONS

Manufacturer:

Huizhou Jinsheng Medical Technology Co., Ltd

Luangang Dahu, Shiwan Mingyue 2nd Road, Boluo County, Huizhou, Guangdong, China, 516000

PRINCIPAL DISPLAY PANEL

See Label

INGREDIENTS AND APPEARANCE

0.9 PERCENTSALINE 
sodium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87311-101
Route of Administration	OPHTHALMIC, NASAL, TOPICAL, CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	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: 87311-101-02	20 in 1 BOX	02/03/2026
1	NDC: 87311-101-01	15 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/03/2026

Labeler - Huizhou Jinsheng Medical Technology Co., Ltd (715285481)

Registrant - Huizhou Jinsheng Medical Technology Co., Ltd (715285481)

Establishment
Name	Address	ID/FEI	Business Operations
Huizhou Jinsheng Medical Technology Co., Ltd		715285481	label(87311-101) , manufacture(87311-101)