Home NDC 71192-030-02 WKND UNDERWATER SUN WHITE
Product NDC 71192-030
Requested package NDC 71192-030-02
11-digit product format 711920030
Labeler code 71192
Product ID 71192-030_a5595583-af14-4f08-a0ec-23567c85b15f
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Octocrylene, Homosalate, Octisalate, Avobenzone
Dosage form STICK
Route TOPICAL
Labeler SURFCODE
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-12-01
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; OCTOCRYLENE; HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength 4 g/18g; g/18g; g/18g; g/18g; g/18g
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71192-030-01 WKND UNDERWATER SUN WHITE 18 g in 1 CONTAINER STICK 18 2 71192-030-02 WKND UNDERWATER SUN WHITE 1 in 1 CARTON STICK 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71192-030 WKND UNDERWATER SUN WHITE (TITANIUM DIOXIDE, OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE) STICK [SURFCODE] 2 Legacy NDC, 2 package rows 20191223_0c30c05d-e76b-472e-ad0c-22723d353d95.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71192-030-02 71192003002 1 CONTAINER in 1 CARTON (71192-030-02) > 18 g in 1 CONTAINER (71192-030-01) 1 container 2017-12-01 0000-00-00 No No Current