FDA.reportPublic FDA data

Victoria Bay

Manufacturer
Midlab Incorporated
Effective date
2018-11-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:45:08

Label at a glance#

ProductVictoria Bay
Active ingredientCHLOROXYLENOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal package displayPrincipal package display

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

OTC - PURPOSE SECTION

PurposePurpose

INDICATIONS & USAGE SECTION

UsesUses

WARNINGS SECTION

WarningWarning

OTC - ASK DOCTOR SECTION

DoctorDoctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOOROCKOOROC

DOSAGE & ADMINISTRATION SECTION

DosageDosage

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70542-30470542-304-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
CHLOROXYLENOL0F32U78V2QACTIB
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM SULFATE0YPR65R21JIACT
TRIMETHYLENEDIAMINETETRAACETIC ACID3F6OA94EERIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
GLYCOL STEARATE0324G66D0EIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT

Source Document#

Source XML · Source PDF

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
c9759dcb-11e8-8813-e053-2a95a90af63446cbc151-30bb-4ad4-e054-00144ff88e882021-08-13WarningsExact identifier
spl set id: 46cbc151-30bb-4ad4-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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