Home NDC 72727-0001 Alcohol Prep Pad-Large
Product NDC 72727-0001
11-digit product format 727270001
Labeler code 72727
Product ID 72727-0001_637c6cf2-f2a4-414a-86f5-d7ca4b5f975b
Type HUMAN OTC DRUG
Nonproprietary name ISOPROPYL ALCOHOL
Dosage form SWAB
Route TOPICAL
Labeler Global Biomedical Technologies, LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-20
Marketing end 2027-02-01
Substance ISOPROPYL ALCOHOL
Active strength .7 mL/mL
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 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 72727-0001 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72727-0001 72727-0001-2 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 Pad-Large Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL .7 mL/mL
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 72727-0001-2 Alcohol Prep Pad-Large 20 in 1 BOX SWAB 20 8 72727-0001-2 Alcohol Prep Pad-Large 0.4 mL in 1 POUCH SWAB 0.4 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72727-0001 ALCOHOL PREP PAD-LARGE (ISOPROPYL ALCOHOL) SWAB [GLOBAL BIOMEDICAL TECHNOLOGIES, LLC
] 8 Current NDC, Legacy NDC, 2 package rows 20250114_93d00515-e93f-48a3-b66b-7d933e734e54.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 72727-0001-2 72727000102 20 POUCH in 1 BOX (72727-0001-2) / .4 mL in 1 POUCH 20 pouch 2019-03-20 2027-02-01 No No Current