Home NDC 71241-001-10 BIOCORNEUM PLUS SPF 30 ADVANCED SCAR TREATMENT
Product NDC 71241-001
Requested package NDC 71241-001-10
11-digit product format 712410001
Labeler code 71241
Product ID 71241-001_5f3bc292-f692-998a-e053-2a91aa0a1782
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate Octisalate Octocrylene Oxybenzone
Dosage form GEL
Route TOPICAL
Labeler SIENTRA, INC.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-03-09
Marketing end 0000-00-00
Substance OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength 8 g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2020-12-31
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 2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 71241-001 71241-001-10 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 71241-001 71241-001-10 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 71241-001-10 71241000110 1 BOTTLE, PUMP in 1 CARTON (71241-001-10) > 10 g in 1 BOTTLE, PUMP (71241-001-97) 2016-03-09 0000-00-00 No No Current