Home NDC 64141-024-01 BOBBI BROWN BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 15
Product NDC 64141-024
Requested package NDC 64141-024-01
11-digit product format 641410024
Labeler code 64141
Product ID 64141-024_235f42cd-4cb1-4fbc-a126-3e77e6166dce
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTINOXATE, OCTISALATE, and OCTOCRYLENE
Dosage form SPRAY
Route TOPICAL
Labeler Bobbi Brown Professional Cosmetics Inc.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-01-01
Marketing end 0000-00-00
Substance AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength 0 g/mL; g/mL; g/mL; g/mL
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 · 12 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Marketing start Marketing end Sample Exclude flag Status 64141-024-01 64141002401 1 BOTTLE, SPRAY in 1 CARTON (64141-024-01) > 200 mL in 1 BOTTLE, SPRAY 2017-01-01 0000-00-00 No No Current