FDA.reportPublic FDA data

Isopropyl Rubbing Alcohol 50%

Product NDC
52000-008
Requested package NDC
52000-008-06
11-digit product format
520000008
Labeler code
52000
Product ID
52000-008_ee0c18d1-ab71-8efe-e053-2a95a90ad9b8
Type
HUMAN OTC DRUG
Nonproprietary name
Isopropyl Alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Universal Distribution Center LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-03-13
Marketing end
0000-00-00
Substance
ISOPROPYL ALCOHOL
Active strength
50 mL/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage52000-00852000-008-06IInactivated by FDA2026-10-15

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage52000-00852000-008-06IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage52000-00852000-008-06IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage52000-00852000-008-06IInactivated by FDAexcluded / ndc_excluded.zipfb8cb913e6d1…eb8c232b6be0…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
52000-008-012025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-022025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-032025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-042025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-052025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-062025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-072025-07-29Isopropyl Rubbing Alcohol 50%
52000-008-012022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-022022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-032022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-042022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-052022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-062022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-072022-11-22Isopropyl Rubbing Alcohol 50%
52000-008-012022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-022022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-032022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-042022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-052022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-062022-07-29Isopropyl Rubbing Alcohol 50%
52000-008-072022-07-29Isopropyl Rubbing Alcohol 50%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-008-01Isopropyl Rubbing Alcohol 50%118 mL in 1 BOTTLE, PLASTICLIQUID1185
52000-008-02Isopropyl Rubbing Alcohol 50%177 mL in 1 BOTTLE, PLASTICLIQUID1775
52000-008-03Isopropyl Rubbing Alcohol 50%237 mL in 1 BOTTLE, PLASTICLIQUID2375
52000-008-04Isopropyl Rubbing Alcohol 50%296 mL in 1 BOTTLE, PLASTICLIQUID2965
52000-008-05Isopropyl Rubbing Alcohol 50%355 mL in 1 BOTTLE, PLASTICLIQUID3555
52000-008-06Isopropyl Rubbing Alcohol 50%414 mL in 1 BOTTLE, PLASTICLIQUID4145
52000-008-07Isopropyl Rubbing Alcohol 50%473 mL in 1 BOTTLE, PLASTICLIQUID4735

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302ISOPROPYL RUBBING ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302ISOPROPYL RUBBING ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1
WATERINACTIVE INGREDIENT059QF0KO0RISOPROPYL RUBBING ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-008ISOPROPYL RUBBING ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]5Legacy NDC, 7 package rows20241212_010a9d81-4039-441b-b478-41ccf527e4df.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN010a9d81-4039-441b-b478-41ccf527e4df5
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD010a9d81-4039-441b-b478-41ccf527e4df5
616456isopropyl alcohol 50 % Topical SolutionSY010a9d81-4039-441b-b478-41ccf527e4df5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52000-008-0652000000806414 mL in 1 BOTTLE, PLASTIC (52000-008-06) 414 ml2012-03-130000-00-00NoNoCurrent