Home NDC 63801-107 Bensal HP
Product NDC 63801-107
11-digit product format 638010107
Labeler code 63801
Product ID 63801-107_5bed0a42-3787-4b47-b322-67102bbe6d64
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Salicylic Acid
Dosage form OINTMENT
Route TOPICAL
Labeler SMG Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1998-10-01
Marketing end 0000-00-00
Substance SALICYLIC ACID
Active strength 30 mg/g
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63801-107-01 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63801-107-15 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63801-107-01 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63801-107-15 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 63801-107-01 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 63801-107-15 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 63801-107-01 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 63801-107-15 I Inactivated by FDA 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63801-107 BENSAL HP (SALICYLIC ACID) OINTMENT [SMG PHARMACEUTICALS, LLC ] 9 Legacy NDC 20241122_4b8ccee9-0f26-416d-a6e5-1261408df899.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63801-107-01 63801010701 1 TUBE in 1 CARTON (63801-107-01) > 30 g in 1 TUBE 1 tube 1998-10-01 0000-00-00 No No Current 63801-107-15 63801010715 2 g in 1 TUBE (63801-107-15) 2 g 1998-10-01 0000-00-00 Yes No Current