FDA.reportPublic FDA data

Alcohol Prep Pad

Product NDC
59294-000
11-digit product format
592940000
Labeler code
59294
Product ID
59294-000_eaf7ae40-0fa6-3d92-e053-2995a90ad804
Type
HUMAN OTC DRUG
Nonproprietary name
ISOPROPYL ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Global Healthcare
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2013-07-11
Marketing end
0000-00-00
Substance
ISOPROPYL ALCOHOL
Active strength
70 g/100g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct59294-000DDiscontinued by firm2026-10-05
excluded packagepackage59294-00059294-000-00DDiscontinued by firm2026-10-05

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, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage59294-000-00d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage59294-000-00f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) LIQUID [GLOBAL HEALTHCARE]1
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) LIQUID [GLOBAL HEALTHCARE]1
WATERINACTIVE INGREDIENT059QF0KO0RALCOHOL PREP PAD (ISOPROPYL ALCOHOL) LIQUID [GLOBAL HEALTHCARE]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59294-000ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) LIQUID [GLOBAL HEALTHCARE]4Legacy NDC20231019_f4091ea1-c626-4a63-82e6-ddf116983b5b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59294-000-00592940000001 PATCH in 1 PACKET (59294-000-00) > .4 g in 1 PATCH1 patch2013-07-110000-00-00NoNoCurrent