Home NDC 31645-216-01 Hand sanitizer
Product NDC 31645-216
Requested package NDC 31645-216-01
11-digit product format 316450216
Labeler code 31645
Product ID 31645-216_b2e8a168-1492-1ca9-e053-2a95a90a02ba
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form SPRAY
Route TOPICAL
Labeler Physicians Formula
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-10
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 80 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 · 4 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 2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…
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 31645-216-01 31645021601 26 mL in 1 BOTTLE, SPRAY (31645-216-01) 26 ml 2020-04-10 0000-00-00 No No Current