Home NDC 62032-0140-09 NDC 62032-0140-09 This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
Requested NDC 62032-0140-09
Product root 62032-0140
Identity scope Package
Primary current NDC product row Not present 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 · 8 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 2025-08-27 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…
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 9 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Obagi-C C-Rx System Normal-Dry Skin Intervention HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b 2026-01-26 Warnings Exact identifier ndc11 (package): 62032014009 Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC 321e58d0-9964-4da9-af6b-66ba81b60cf7 2026-01-26 Warnings Exact identifier ndc11 (package): 62032014009 Obagi Nu-Derm Fx System Normal-Oily Skin Transformation Complexion Brightening System HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC 49cd9e72-4e25-4ff9-aefc-467733b105be 2025-10-23 Warnings Exact identifier ndc11 (package): 62032014009 Obagi Nu-Derm System Normal-Dry Skin Transformation Kit HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC 16efa2db-8172-4026-a519-08f53d68b3c9 2025-10-23 Warnings Exact identifier ndc11 (package): 62032014009 Obagi Nu-Derm System Normal-Oily Skin Transformation HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC e63327db-fb96-411c-945a-abe801d38045 2025-10-23 Warnings Exact identifier ndc11 (package): 62032014009 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit Complexion Brightening System HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC cead2b1c-671d-45f9-b450-2827128792fe 2025-10-23 Warnings Exact identifier ndc11 (package): 62032014009 Obagi-C C-Rx System Normal-Oily Skin Intervention HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE Obagi Cosmeceuticals LLC e19b824f-4438-48c8-af4c-29be197f9cdc 2025-10-21 Warnings Exact identifier ndc11 (package): 62032014009 Obagi Skintrinsiq Brightening Protocol HOMOSALATE, OCTISALATE, AND ZINC OXIDE Obagi Cosmeceuticals LLC 2f75ebf7-d6b6-45c6-ad5b-61739d260ff7 2025-03-21 Warnings Exact identifier ndc11 (package): 62032014009 SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN HOMOSALATE, OCTISALATE, AND ZINC OXIDE Obagi Cosmeceuticals LLC 263ef8e8-e0c4-42e6-bb26-7581a437b35a 2025-03-14 Warnings Exact identifier ndc11 (package): 62032014009
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.