FDA.reportPublic FDA data

Description for Bacteriostatic Water

Manufacturer
Fujian Genohope Biotech Ltd.
Effective date
2026-06-23
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:39:45

Label at a glance#

ProductBacteriostatic Water
Active ingredientWATER
Label structure4 sections

Label contents#

Full prescribing information#

Description for Bacteriostatic Water

DESCRIPTION SECTION

Description for Bacteriostatic WaterDescription for Bacteriostatic Water

HOW SUPPLIED SECTION

Bacteriostatic Water for Injection is supplied as 30 mL multiple-dose vials (NDC 84502-115-01), packaged 25 vials per carton (NDC 84502-115-02). Each carton contains twenty-five 30 mL vials.

Carton label for Bacteriostatic Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton label for Bacteriostatic WaterCarton label for Bacteriostatic Water

Vial_Label_Bacteriostatic_Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vial_Label_Bacteriostatic_WaterVial_Label_Bacteriostatic_Water

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84502-11584502-115-01, 84502-115-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHIACT
WATER059QF0KO0RACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bacteriostatic WaterBACTERIOSTATIC WATERFujian Genohope Biotech Ltd.54f66b82-c9e5-a2bc-e063-6394a90adbbc2026-06-23Exact identifier
ndc (package): 84502-115-02
ndc (package): 84502-115-01
ndc (product): 84502-115
ndc11 (package): 84502011502
ndc11 (package): 84502011501
spl id: 54f66ba5-5bb2-3927-e063-6294a90ab7fb
spl set id: 54f66b82-c9e5-a2bc-e063-6394a90adbbc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.