Home NDC 61354-084 Cream
Product NDC 61354-084
11-digit product format 613540084
Labeler code 61354
Product ID 61354-084_e7763ac1-d05c-7f8f-e053-2995a90a6c15
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form CREAM
Route TOPICAL
Labeler Oxygen Development LLC
Application M020
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-08-30
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 5 mg/100mg; mg/100mg
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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 61354-084-01 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 61354-084-01 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 61354-084-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 61354-084-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 61354-084-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 61354-084-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 61354-084-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 61354-084-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 61354-084-01 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 61354-084-01 Cream 100 mg in 1 TUBE CREAM 100 1 61354-084-01 Cream 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61354-084 CREAM (ZINC OXIDE, TITANIUM DIOXIDE) CREAM [OXYGEN DEVELOPMENT LLC] 1 Legacy NDC, 2 package rows 20220831_e7760899-8b4a-9a2a-e053-2995a90a2fd5.zip
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 264 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join I Conceal Flawless Foundation Broad Spectrum SPF 30 Sunscreen Mahogany ZINC OXIDE AND TITANIUM DIOXIDE Allure Labs dcba05ff-7a68-c5c0-e053-2a95a90a6129 2024-12-09 Warnings Exact identifier application number: M020 Prevention Daily Matte Moisturizer SPF 30 ZINC OXIDE AND HOMOSALATE Allure Labs f0fb1b69-53f2-efff-e053-2995a90af9d4 2024-12-09 Warnings Exact identifier application number: M020 MD Restoring daily Defense Moisturizer SPF 50 ZINC OXIDE AND TITANIUM DIOXIDE Allure Labs Inc eb8e7109-b5eb-5cc1-e053-2995a90a486f 2024-12-09 Warnings Exact identifier application number: M020 Prevention Sun Serum SPF 30 Tinted ZINC OXIDE Allure Labs f1761b09-9061-a052-e053-2a95a90a39c8 2024-12-09 Warnings Exact identifier application number: M020 Prevention Sun Serum SPF30 ZINC OXIDE Allure Labs f188669f-7b9f-6e01-e053-2995a90afa3c 2024-12-09 Warnings Exact identifier application number: M020 Prevention Clear Solar Gel SPF30 AVOBENZON, OCTISALATE AND OCTOCRYLENE Allure LAbs f19f6d9b-5249-27a6-e053-2a95a90a8a39 2024-12-09 Warnings Exact identifier application number: M020 OneSkin OS-01 SHIELD Broad Spectrum SPF 30 Mineral Sunscreen Tinted ZINC OXIDE Allure Labs 02e7fb00-2039-c4f8-e063-6294a90a418f 2024-12-09 Warnings Exact identifier application number: M020 OneSkin OS-01 SHIELD Broad Spectrum SPF 30 Mineral Sunscreen Untinted ZINC OXIDE Allure Labs 02f9c859-8d7d-5146-e063-6394a90a57b5 2024-12-09 Warnings Exact identifier application number: M020 Quench and Protect Hydrating SPF30 ZINC DIOXIDE AND TITANIUM DIOXIDE Allure Labs. 039e50c1-7b3d-d392-e063-6394a90a4b3c 2024-12-09 Warnings Exact identifier application number: M020 Tinted Face Cream SPF 15 OCTOCRYLENE, OCTISALATE Bentley Laboratories, LLC 0d7300ee-adf4-41be-bb9f-257cd2986c0f 2024-12-06 Warnings Exact identifier application number: M020 Derm Institute Daily Defense Protection Sunscreen Broad Spectrum SPF50 TITANIUM DIOXIDE, ZINC OXIDE Beautcella Inc. bad942d8-04da-31d2-e053-2a95a90a9275 2024-12-06 Warnings Exact identifier application number: M020 TOM FORD ARCHITECTURE RADIANCE HYDRATING FOUNDATION BROAD SPECTRUM SPF 50 ENSULIZOLE, OCTINOXATE, OCTISALATE, AND ZINC OXIDE TOM FORD BEAUTY DIST 289b824f-bb0b-313e-e063-6394a90ab783 2024-12-06 Warnings Exact identifier application number: M020 ATTITUDE Sunly Mineral Sunscreen Stick Orange Blossom SPF 30 ZINC OXIDE 9055-7588 Quebec Inc. DBA Attitude 0d840001-a648-df1b-e063-6294a90ab299 2024-12-06 Warnings Exact identifier application number: M020 Performance Face Sunscreen Broad Spectrum SPF 30 ZINC OXIDE, OCTOCRYLENE, OCTISALATE Bentley Laboratories, LLC 1629f061-b8fc-4fda-8378-c64e164d41bd 2024-12-06 Warnings Exact identifier application number: M020 Clear System Brightening Day Cream SPF 15 OCTOCRYLENE, OCTISALATE Bentley Laboratories, LLC 8cbc8fa4-469f-4fa3-bd8e-27e815989c3f 2024-12-06 Warnings Exact identifier application number: M020 MISSHA M Perfect Cover BB Cream SPF42 (No. 25) ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE Able C&C Co., Ltd. 604e7a49-7986-11ee-e053-2a91aa0a1bee 2024-12-05 Warnings Exact identifier application number: M020 MISSHA M Perfect Cover BB No 27 ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE Able C&C Co., Ltd. c4e16cec-c7db-4e5e-9d05-5d7afdb79091 2024-12-05 Warnings Exact identifier application number: M020 MISSHA M Perfect Cover BB SPF42 No29 OCTINOXATE, ZINC OXIDE, TITANIUM DIOXIDE Able C&C Co., Ltd. 3fc90114-4cdf-273e-e054-00144ff8d46c 2024-12-05 Warnings Exact identifier application number: M020 MISSHA M Perfect Cover BB No 31 ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE Able C&C Co., Ltd. 95862d15-d977-7276-e053-2995a90ab690 2024-12-05 Warnings Exact identifier application number: M020 MISSHA M Perfect Cover BB Cream SPF42 No. 25 ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE Able C&C Co., Ltd. 9c6f48b1-007b-434f-b756-242e3390e9b7 2024-12-05 Warnings Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61354-084-01 61354008401 1 TUBE in 1 CARTON (61354-084-01) > 100 mg in 1 TUBE 1 tube 2022-08-30 0000-00-00 No No Current