Home NDC 58832-0005-2 LAPOTHICELL Sunscreen
Product NDC 58832-0005
Requested package NDC 58832-0005-2
11-digit product format 588320005
Labeler code 58832
Product ID 58832-0005_adb00a53-eb6d-22f2-e053-2995a90af52e
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Bemotrizinol, Ethylhexyl Triazone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler EYESOME. Co.,Ltd.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-06-20
Marketing end 0000-00-00
Substance HOMOSALATE; OCTISALATE; AVOBENZONE; BEMOTRIZINOL; OCTOCRYLENE; ETHYLHEXYL TRIAZONE
Active strength 5 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL
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 · 19 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…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58832-0005-1 LAPOTHICELL Sunscreen 50 mL in 1 TUBE CREAM 50 1 58832-0005-2 LAPOTHICELL Sunscreen 2 in 1 CARTON CREAM 2 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58832-0005 LAPOTHICELL SUNSCREEN (AVOBENZONE, BEMOTRIZINOL, ETHYLHEXYL TRIAZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [EYESOME. CO.,LTD.] 1 Legacy NDC, 2 package rows 20200826_adb00a53-eb6c-22f2-e053-2995a90af52e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58832-0005-2 58832000502 2 TUBE in 1 CARTON (58832-0005-2) > 50 mL in 1 TUBE (58832-0005-1) 2 tube 2020-08-25 0000-00-00 No No Current