Home NDC 80376-001-01 Sunblock Cream
Product NDC 80376-001
Requested package NDC 80376-001-01
11-digit product format 803760001
Labeler code 80376
Product ID 80376-001_ae288ef6-d4ec-1bb9-e053-2995a90aa216
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler Zhuhai Yasha Medical Instrument Co., Ltd.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-08-31
Marketing end 0000-00-00
Substance OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 9 g/100g; g/100g; 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 · 18 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…
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 80376-001-01 Sunblock Cream 50 g in 1 BOTTLE CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80376-001 SUNBLOCK CREAM (ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE) CREAM [ZHUHAI YASHA MEDICAL INSTRUMENT CO., LTD.] 1 Legacy NDC, 1 package rows 20200901_ae288ef6-d4eb-1bb9-e053-2995a90aa216.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80376-001-01 80376000101 50 g in 1 BOTTLE (80376-001-01) 50 g 2020-08-31 0000-00-00 No No Current