Home NDC 20276-053-12 Lucky
Product NDC 20276-053
Requested package NDC 20276-053-12
11-digit product format 202760053
Labeler code 20276
Product ID 20276-053_b8e2c8a6-d3f6-0c13-e053-2995a90a0a11
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Delta Brands Inc.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2012-10-30
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 1 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 2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 20276-053 20276-053-12 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 20276-053-12 20276005312 355 mL in 1 BOTTLE, PUMP (20276-053-12) 355 ml 2012-10-30 0000-00-00 No No Current