Home NDC 70900-202-54 SUNSHIELD
Product NDC 70900-202
Requested package NDC 70900-202-54
11-digit product format 709000202
Labeler code 70900
Product ID 70900-202_d4f149fb-a0c9-5687-e053-2a95a90abef0
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler CLINICAL CARE SKIN SOLUTIONS, INC
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-08-04
Marketing end 0000-00-00
Substance OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength 7 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2023-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 70900-202-14 SUNSHIELDSPF-30 120 mL in 1 BOTTLE CREAM 120 7 70900-202-54 SUNSHIELDSPF-30 1 in 1 BOX CREAM 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70900-202 SUNSHIELD SPF-30 (OCTINOXATE, OCTISALATE, ZINC OXIDE) CREAM [CLINICAL CARE SKIN SOLUTIONS, INC] 7 Legacy NDC, 2 package rows 20230222_e20506af-5801-4e11-b963-52916afbda01.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70900-202-54 70900020254 1 BOTTLE in 1 BOX (70900-202-54) > 120 mL in 1 BOTTLE (70900-202-14) 1 bottle 2016-08-04 0000-00-00 No No Current