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 286 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join H.E.B Solutions Sunscreen KIDS SPF 50 LOTION SPRAY H.E.B 9b43c5d5-c279-4ae3-843e-1451f7324216 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 2e183ba8-1b83-4211-bc08-dbdcee942ce9 2024-10-15 Warnings Exact identifier application number: M020 EQUALINE KIDS SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE United Natural Foods, Inc. dba UNFI e46cb6e3-ea8d-3c2d-e053-2a95a90a0bf6 2024-10-15 Warnings Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE SUNSCREEN Bentley Laboratories LLC 782a8641-7e6a-413b-a2ed-0efeb36c48a7 2024-10-15 Warnings Exact identifier application number: M020 H.E.B MANGO SPF 50 SUNSCREEN H.E.B 35898f07-2973-461a-91b8-095aa4cf38ee 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 30 CONTINUOUS SPRAY H.E.B 8b6d0c0d-485b-4428-91e5-5befcac18d5d 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 5fd3d730-d916-48f4-bb94-62d40d181280 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 70 CONTINUOUS SPRAY H.E.B f9b5b360-6b69-4006-934f-5bc8a9fdfcd0 2024-10-15 Warnings Exact identifier application number: M020 HEB GENERAL PROTECTION SPF 100 LOTION H-E-B 39d94e3a-98c8-44b0-bd2d-f318ac7bbf75 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen WET PROTECTION KIDS SPF 70 CONTINUOUS SPRAY H.E.B f823b236-5884-41d9-bff0-65b91664aaad 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen COOLING SPORT SPF 50 CONTINUOUS SPRAY H.E.B 67fdf3a0-08fe-4348-a4f9-a83f3cf46b72 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 70 CONTINUOUS SPRAY H.E.B c16935ce-afdb-4571-b5a3-6dc5d01f721c 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen BABY SPF 50 LOTION SPRAY H.E.B 1082111f-bf04-4a98-b6a0-5da933652f1d 2024-10-15 Warnings Exact identifier application number: M020 H.E.B ULTRA SPF 50 SUNSCREEN H.E.B d6184ba2-0e47-459a-8777-1f27be2140a6 2024-10-15 Warnings Exact identifier application number: M020 H.E.B ULTRA SPF 30 SUNSCREEN H.E.B 90287874-cdfa-489c-936d-e487f6b3db96 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 2c9258ac-8cbe-4acf-9c02-bb993d69a3e5 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 39bf1379-3dee-4aa0-967a-36faccca4216 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 100 CONTINUOUS SPRAY H.E.B 301ae7e5-5a60-45d0-8cd5-553ba07db4c5 2024-10-15 Warnings Exact identifier application number: M020 Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 28C HOMOSALATE, ZINC OXIDE Rare Beauty, LLC 2470d78c-724f-4181-e063-6294a90afeaa 2024-10-14 Warnings Exact identifier application number: M020 Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 44N HOMOSALATE, ZINC OXIDE Rare Beauty, LLC 2471e0fa-ddc8-1c62-e063-6294a90a4408 2024-10-14 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