Home NDC 62032-160-10 Obagi
Product NDC 62032-160
Requested package NDC 62032-160-10
11-digit product format 620320160
Labeler code 62032
Product ID 62032-160_aba674be-7709-4424-a7cb-180319280978
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octinoxate, Titanium dioxide, Zinc oxide
Dosage form LOTION
Route TOPICAL
Labeler Obagi Cosmeceuticals LLC
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2019-12-01
Marketing end 0000-00-00
Substance HOMOSALATE; OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 9 g/85g; g/85g; g/85g; g/85g
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 · 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62032-160-10 ObagiSun Shield TINT Warm Sunscreen Broad Spectrum SPF 50 1 in 1 CARTON LOTION 1 3 62032-160-10 ObagiSun Shield TINT Warm Sunscreen Broad Spectrum SPF 50 85 g in 1 TUBE LOTION 85 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-160 OBAGI SUN SHIELD TINT WARM SUNSCREEN BROAD SPECTRUM SPF 50 (HOMOSALATE, OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE) LOTION [OBAGI COSMECEUTICALS LLC] 3 Legacy NDC, 2 package rows 20210213_b1aacb4d-7ede-4aae-8d6a-afff2a057e46.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-160-10 62032016010 1 TUBE in 1 CARTON (62032-160-10) > 85 g in 1 TUBE 1 tube 2019-12-01 0000-00-00 No No Current