FDA.reportPublic FDA data

Maxim

Manufacturer
Midlab Incorporated
Effective date
2023-03-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:33:51

Label at a glance#

ProductMaxim
Active ingredientCHLOROXYLENOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

OTC - PURPOSE SECTION

PurposePurpose

INDICATIONS & USAGE SECTION

UsesUses

WARNINGS SECTION

WarningsWarnings

OTC - ASK DOCTOR SECTION

Ask DoctorAsk Doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOOROCKOOROC

DOSAGE & ADMINISTRATION SECTION

Dosage and AdminDosage and Admin

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70542-60170542-601-41, 70542-601-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM LAURETH SULFATEBPV390UAP0IACT
LAURAMINE OXIDE4F6FC4MI8WIACT
FD&C RED NO. 40WZB9127XOAIACT
CHLOROXYLENOL0F32U78V2QACTIB
FD&C YELLOW NO. 5I753WB2F1MIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT

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
f7e7d0f7-229e-3082-e053-6394a90a0d5883d29fb9-3398-c55e-e053-2991aa0a32a72023-03-27WarningsExact identifier
spl id: f7e7d0f7-229e-3082-e053-6394a90a0d58
spl set id: 83d29fb9-3398-c55e-e053-2991aa0a32a7

Reported adverse events (FAERS/openFDA)#

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