Home NDC 75936-505-06 Super Power Sunscreen Mousse SPF 50
Product NDC 75936-505
Requested package NDC 75936-505-06
11-digit product format 759360505
Labeler code 75936
Product ID 75936-505_2d35d40a-0a7a-4246-8029-705bbd89e350
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octinoxate, Octisalate
Dosage form CREAM
Route TOPICAL
Labeler TAYLOR JAMES, LTD.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-01-13
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE
Active strength 3 kg/100mL; kg/100mL; kg/100mL; kg/100mL
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 · 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75936-505-01 Super Power Sunscreen Mousse SPF 50Supergoop 100 mL in 1 TUBE CREAM 100 2 75936-505-02 Super Power Sunscreen Mousse SPF 50Supergoop 1 in 1 BOX CREAM 1 2 75936-505-03 Super Power Sunscreen Mousse SPF 50Supergoop 210 mL in 1 TUBE CREAM 210 2 75936-505-04 Super Power Sunscreen Mousse SPF 50Supergoop 1 in 1 BOX CREAM 1 2 75936-505-05 Super Power Sunscreen Mousse SPF 50Supergoop 50 mL in 1 CAN CREAM 50 2 75936-505-06 Super Power Sunscreen Mousse SPF 50Supergoop 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75936-505 SUPER POWER SUNSCREEN MOUSSE SPF 50 SUPERGOOP (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE) CREAM [TAYLOR JAMES, LTD.] 2 Legacy NDC, 6 package rows 20180210_0a7bf045-d6cc-4321-9480-4f0841b314b7.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75936-505-06 75936050506 1 CAN in 1 BOX (75936-505-06) > 50 mL in 1 CAN (75936-505-05) 1 can 2018-02-07 0000-00-00 No No Current