Home NDC 76162-809-30 Alcohol Prep
Product NDC 76162-809
Requested package NDC 76162-809-30
11-digit product format 761620809
Labeler code 76162
Product ID 76162-809_0d7ffc64-5322-ba5d-e063-6294a90a6cac
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form SWAB
Route TOPICAL
Labeler Topco Associates
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-07-13
Marketing end 2026-12-31
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Current FDA listing Yes 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 76162-809 76162-809-30 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 76162-809 76162-809-30 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Alcohol Prep Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ND2M416302 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 797544 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76162-809-30 Alcohol Prep 1 in 1 PACKET SWAB 1 7 76162-809-30 Alcohol Prep 100 in 1 BOX SWAB 100 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76162-809 ALCOHOL PREP (ISOPROPYL ALCOHOL) SWAB [TOPCO ASSOCIATES] 7 Current NDC, Legacy NDC, 2 package rows 20231228_65270825-48b1-49e7-a14e-f73df9beb9dd.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 9 of 115 · 2,286 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76162-809-30 76162080930 100 PACKET in 1 BOX (76162-809-30) / 1 APPLICATOR in 1 PACKET / .5 mL in 1 APPLICATOR 100 packet 2011-07-13 2026-12-31 No No Current