FDA.reportPublic FDA data

Alcohol

Product NDC
11673-826
11-digit product format
116730826
Labeler code
11673
Product ID
11673-826_4ffdb678-aabd-4d99-e063-6394a90ac0b8
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Target Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-10-13
Substance
ALCOHOL
Active strength
62 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage11673-82611673-826-34DDiscontinued by firm2026-08-07
excluded packagepackage11673-82611673-826-45DDiscontinued by firm2026-08-07

Additional Listing Data#

Finished product
Yes
Brand name base
Alcohol
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
247835Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5c6be1e4-ae02-430c-8ed7-2148660da19dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-826-16Alcohol59 mL in 1 BOTTLE, PLASTICLIQUID5910
11673-826-34Alcohol237 mL in 1 BOTTLE, PLASTICLIQUID23710
11673-826-45Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID94610

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-826ALCOHOL LIQUID [TARGET]7Current NDC, Legacy NDC, 3 package rows20240726_5c6be1e4-ae02-430c-8ed7-2148660da19d.zip

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
AlcoholALCOHOLTarget Corporation5c6be1e4-ae02-430c-8ed7-2148660da19d2026-04-21Warnings, Adverse reactionsExact identifier
ndc (product): 11673-826

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
247835ethanol 62 % Topical SolutionPSN5c6be1e4-ae02-430c-8ed7-2148660da19d10
247835ethanol 0.62 ML/ML Topical SolutionSCD5c6be1e4-ae02-430c-8ed7-2148660da19d10
247835ethanol 62 % Topical SolutionSY5c6be1e4-ae02-430c-8ed7-2148660da19d10
247835ethyl alcohol 62 % Topical SolutionSY5c6be1e4-ae02-430c-8ed7-2148660da19d10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-826-161167308261659 mL in 1 BOTTLE, PLASTIC (11673-826-16) 59 ml2020-10-130000-00-00NoNoCurrent
11673-826-3411673082634237 mL in 1 BOTTLE, PLASTIC (11673-826-34) 237 ml2020-10-130000-00-00NoNoCurrent
11673-826-4511673082645946 mL in 1 BOTTLE, PLASTIC (11673-826-45) 946 ml2020-10-130000-00-00NoNoCurrent