FDA.reportPublic FDA data

Molluscum Contagiosum Treatment

Manufacturer
Good Manager Holdings Inc
Effective date
2023-07-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:27:33

Label at a glance#

ProductMolluscum Contagiosum Treatment
Active ingredientSALICYLIC ACID
Label structure13 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTSINACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTACTIVE INGREDIENT

OTC - DO NOT USE SECTION

DO NOT USEDO NOT USE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

OTC - PURPOSE SECTION

PURPOSEPURPOSE

OTC - STOP USE SECTION

STOP USESTOP USE

DOSAGE & ADMINISTRATION SECTION

DOSAGEDOSAGE

WARNINGS SECTION

WARNINGWARNING

OTC - WHEN USING SECTION

WHEN USINGWHEN USING

OTHER SAFETY INFORMATION

OTHER INFORMATIONOTHER INFORMATION

OTC - ASK DOCTOR SECTION

ASK DOCTORASK DOCTOR

INDICATIONS & USAGE SECTION

USAGEUSAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELPACKAGE LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82372-006-012025-02-12C16284748780-12cef2736-68ff-d83d-e063-dadaa90ab31f016e9d99-5417-b42f-e063-6394a90acc8d
82372-006-012025-01-30C16284748780-12cef2736-68ff-d83d-e063-dadaa90ab31f016e9d99-5417-b42f-e063-6394a90acc8d

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
82372-00682372-006-01

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
WATER059QF0KO0RIACT
CHLORHEXIDINE ACETATE5908ZUF22YIACT
ALOE VERA LEAFZY81Z83H0XIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
ALCOHOL3K9958V90MIACT
SALICYLIC ACIDO414PZ4LPZACTIB
STEMONA JAPONICA ROOTFXG254HF10IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
PHELLODENDRON CHINENSIS BARK2866QMZ434IACT

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
2dea9589-6356-37ab-e063-6394a90a36d4016e9d99-5417-b42f-e063-6394a90acc8d2025-02-11WarningsExact identifier
spl set id: 016e9d99-5417-b42f-e063-6394a90acc8d

Reported adverse events (FAERS/openFDA)#

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