Home NDC 78169-040-01 Hand Sanitizer
Product NDC 78169-040
Requested package NDC 78169-040-01
11-digit product format 781690040
Labeler code 78169
Product ID 78169-040_a67df6ac-f5f2-1ad0-e053-2995a90a68ff
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler Industrias Ripian, S.A. de C.V.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-30
Marketing end 0000-00-00
Substance ISOPROPYL ALCOHOL
Active strength 75 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
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 · 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 2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 78169-040 78169-040-01 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 78169-040 78169-040-01 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 78169-040-01 78169004001 1000 mL in 1 BOTTLE (78169-040-01) 1000 ml 2020-03-30 0000-00-00 No No Current