Home NDC 81368-5550-3 Dynamic Broad Spectrum Sunscreen SPF 55
Product NDC 81368-5550
Requested package NDC 81368-5550-3
11-digit product format 813685550
Labeler code 81368
Product ID 81368-5550_b814aced-faad-80c9-e053-2995a90a83a1
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate and Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler National Hair Loss LLC
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-01-04
Marketing end 0000-00-00
Substance OCTINOXATE; ZINC OXIDE
Active strength 75 mg/g; 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 · 15 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…
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 81368-5550-3 Dynamic Broad Spectrum Sunscreen SPF 55 50 g in 1 BOTTLE, PLASTIC CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81368-5550 DYNAMIC BROAD SPECTRUM SUNSCREEN SPF 55 (OCTINOXATE AND ZINC OXIDE) CREAM [NATIONAL HAIR LOSS LLC] 1 Legacy NDC, 1 package rows 20210105_b814aef4-7717-6040-e053-2995a90a30ab.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81368-5550-3 81368555003 50 g in 1 BOTTLE, PLASTIC (81368-5550-3) 50 g 2021-01-04 0000-00-00 No No Current