0.9%SALINE- sodium chloride solution

0.9%saline by

Drug Labeling and Warnings

0.9%saline 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

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

Warnings:
1.Apply the cleaning solution to the area to be cleaned.
2.The product comes in single-use vials, 5 mL each.
3.Not for injection.
4.Do not share or reuse.
5.Keep out of reach of children.
6.Do not use if allergic to any of stated Ingredients, if irritation occurs, discontinue use and consult your doctor or specialist.
7.Use within 24 hours after opening.

8.This product is not a substitute for medication or medical devices.

DOSAGE & ADMINISTRATION

Single use dosage vials 5ml each

ACTIVE INGREDIENT

Active ingredient: Sodium Chloride 0.9%

INACTIVE INGREDIENT

Inactive ingredient: USP Water

OTHER SAFETY INFORMATION

Pay Attention: Do not use if the product is damaged or leaking.

QUESTIONS

Manufacturer:

Huizhou Jinsheng Medical Technology Co., Ltd

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

STORAGE AND HANDLING

Storage:Store at room temperature.Avoid freezing or excessive heat.

PRINCIPAL DISPLAY PANEL

See Label

INGREDIENTS AND APPEARANCE

0.9%SALINE 
sodium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87311-103
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: 87311-103-02	60 in 1 BOX	02/03/2026
1	NDC: 87311-103-01	5 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(87311-103) , manufacture(87311-103)