Home NDC 50232-001-01 Alcohol Prep Pad
Product NDC 50232-001
Requested package NDC 50232-001-01
11-digit product format 502320001
Labeler code 50232
Product ID 50232-001_da8c66a5-0ede-c996-e053-2995a90ad4d2
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form SWAB
Route TOPICAL
Labeler BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.
Application part344
Marketing category OTC MONOGRAPH FINAL
Marketing start 2012-05-14
Marketing end 0000-00-00
Substance ISOPROPYL ALCOHOL
Active strength 1 mL/mL
NDC exclude flag No
Listing certified through 2023-12-31
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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 50232-001-01 50232000101 5000 POUCH in 1 CONTAINER (50232-001-01) > .35 mL in 1 POUCH 5000 pouch 2018-01-01 0000-00-00 No No Current