FDA.reportPublic FDA data

4oz Alcohol

Manufacturer
Collective Science Integration | P&P International
Effective date
2020-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:47

Label at a glance#

Product4oz Alcohol
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DosageDosage

INACTIVE INGREDIENT SECTION

InactiveInactive

INDICATIONS & USAGE SECTION

UsageUsage

OTC - ACTIVE INGREDIENT SECTION

ActiveActive

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachKeep out of reach

OTC - PURPOSE SECTION

PurposePurpose

WARNINGS SECTION

WarningsWarnings

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90055-213-042022-01-28C16284748780-1d6a99b39-cdb5-a426-e053-dadaa90af4c2b1cda2c1-a045-e164-e053-2995a90af58e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90055-213-044oz Alcohol120 mL in 1 BOTTLESOLUTION1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90055-2134OZ ALCOHOL SOLUTION [COLLECTIVE SCIENCE INTEGRATION]1Legacy NDC, 1 package rows20201209_b1cda2c1-a045-e164-e053-2995a90af58e.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90055-21390055-213-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

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
b1cda2c1-a046-e164-e053-2995a90af58eb1cda2c1-a045-e164-e053-2995a90af58e2020-10-16WarningsExact identifier
spl id: b1cda2c1-a046-e164-e053-2995a90af58e
spl set id: b1cda2c1-a045-e164-e053-2995a90af58e

Reported adverse events (FAERS/openFDA)#

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