Home NDC 69638-060-32 Scotts Select Topical Anesthetic
Product NDC 69638-060
Requested package NDC 69638-060-32
11-digit product format 696380060
Labeler code 69638
Product ID 69638-060_8a3b8909-dd8f-4272-8bf8-88d16b253eb8
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route DENTAL; ORAL
Labeler Scott's Dental Supply LLC
Application part356
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-07-23
Marketing end 0000-00-00
Substance BENZOCAINE
Active strength 20 g/100g
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, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA 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 69638-060-32 69638006032 32 g in 1 BOTTLE (69638-060-32) 32 g 2017-07-23 0000-00-00 No No Current