FDA.reportPublic FDA data

Allure Isopropyl Rubbing Alcohol

Product NDC
52000-001
Requested package NDC
52000-001-05
11-digit product format
520000001
Labeler code
52000
Product ID
52000-001_6dffaf6a-8fa0-4606-a9d9-39929810082f
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
2012-06-29
Marketing end
0000-00-00
Substance
ISOPROPYL ALCOHOL
Active strength
50 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 packagepackage52000-00152000-001-05IInactivated by FDA2026-10-12

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 · 4 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2020-06-10 20:45 UTC · source 2020-06-10IInactivated by FDA9bebd1f3094a…5416666fcb17…
2019-12-08 06:16 UTC · source 2019-12-05EExcluded after deficient or non-compliant submission was not corrected110d247fa046…a55b01930146…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
52000-001-012025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-022025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-032025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-042025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-052025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-062025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-072025-07-29ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-012020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-022020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-032020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-042020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-052020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-062020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-072020-08-13ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-012020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-022020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-032020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-042020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-052020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-062020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL
52000-001-072020-01-31ALLURE ISOPROPYL RUBBING ALCOHOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-001-01Allure Isopropyl Rubbing Alcohol118 mL in 1 BOTTLE, PLASTICLIQUID1183
52000-001-02Allure Isopropyl Rubbing Alcohol177 mL in 1 BOTTLE, PLASTICLIQUID1773
52000-001-03Allure Isopropyl Rubbing Alcohol237 mL in 1 BOTTLE, PLASTICLIQUID2373
52000-001-04Allure Isopropyl Rubbing Alcohol296 mL in 1 BOTTLE, PLASTICLIQUID2963
52000-001-05Allure Isopropyl Rubbing Alcohol355 mL in 1 BOTTLE, PLASTICLIQUID3553
52000-001-06Allure Isopropyl Rubbing Alcohol414 mL in 1 BOTTLE, PLASTICLIQUID4143
52000-001-07Allure Isopropyl Rubbing Alcohol473 mL in 1 BOTTLE, PLASTICLIQUID4733

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302ALLURE ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302ALLURE ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1
WATERINACTIVE INGREDIENT059QF0KO0RALLURE ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-001ALLURE ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]3Legacy NDC, 7 package rows20241215_73ad28c6-71e6-41df-a9a2-22834ccef107.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN73ad28c6-71e6-41df-a9a2-22834ccef1073
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD73ad28c6-71e6-41df-a9a2-22834ccef1073
616456isopropyl alcohol 50 % Topical SolutionSY73ad28c6-71e6-41df-a9a2-22834ccef1073

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52000-001-0552000000105355 mL in 1 BOTTLE, PLASTIC (52000-001-05) 355 ml2012-06-290000-00-00NoNoCurrent