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 127 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE BASS & KLASS, INC 36af24e2-015a-a9a7-e063-6294a90a2fce 2025-12-15 Exact identifier application number: M020 Tinted Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE BASS & KLASS, INC 36add3a3-f1ff-3986-e063-6394a90ab7fe 2025-12-15 Exact identifier application number: M020 Antioxidant Mineral Sunscreen Plus Primer Lightly Tinted ZINC OXIDE True Beauty Brows & Skin Care 37dc70ba-a6bb-fe09-e063-6394a90a5129 2025-12-15 Exact identifier application number: M020 COOLA BARE REPUBLIC CLEARSCREEN SPF50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE COOLA, LLC bcbab676-fbe2-f0cc-e053-2a95a90ad4d2 2025-12-15 Warnings Exact identifier application number: M020 COOLA BARE REPUBLIC CLEARSCREEN SPF100 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE COOLA, LLC f14cf2b8-b110-1210-e053-2995a90a0102 2025-12-15 Warnings Exact identifier application number: M020 COOLA BARE REPUBLIC CLEARSCREEN SPF100 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE COOLA, LLC f1504311-4865-5499-e053-2995a90acdcd 2025-12-15 Warnings Exact identifier application number: M020 COOLA BARE REPUBLIC CLEARSCREEN SUNSCREEN SPF100 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE COOLA, LLC f14d70f1-440b-900d-e053-2995a90a30a0 2025-12-15 Warnings Exact identifier application number: M020 REVERSE Brightening Defense Fluid AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE Rodan & Fields dc230e1e-bfb8-4d7c-bad5-bff77d78220e 2025-12-15 Warnings Exact identifier application number: M020 COOLA BARE REPUBLIC MINERAL SPORT SPF50 TITANIUM DIOXIDE, ZINC OXIDE COOLA, LLC bbf15e58-c160-d599-e053-2a95a90a0696 2025-12-14 Warnings Exact identifier application number: M020 Mineral Sunscreen Stick SPF 50 Fragrance-Free ZINC OXIDE COOLA LLC ee8706b0-ad42-403a-be7c-b660f040a244 2025-12-14 Warnings Exact identifier application number: M020 COOLA CLASSIC SUNSCREEN FRAGRANCE FREE AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE COOLA, LLC cfc21b1a-4a26-1573-e053-2995a90a2d50 2025-12-14 Warnings Exact identifier application number: M020 Kopari Sunglaze Sheer Body Mist Sunscreen SPF42 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Kopari Beauty 7c96b799-e24d-473f-8f0a-3fad83d5ed48 2025-12-14 Warnings Exact identifier application number: M020 WOODSLEEP Sunscreen Balm TITANIUM DIOXIDE Shantou Woodsleep Biotechnology Co., Ltd. 45cfc7ed-34a6-1f45-e063-6394a90a902b 2025-12-13 Warnings Exact identifier application number: M020 Universkin by Alma Daily Mineral Serum Broad Spectrum SPF50 ZINC OXIDE 24% UNIVERSKIN 45d242de-cbd8-e7ea-e063-6394a90aaebf 2025-12-13 Warnings Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE SPF 50 ALAINA HEALTHCARE PRIVATE LIMITED b7847d4f-2517-4b58-8e31-676c9d6e484d 2025-12-12 Warnings Exact identifier application number: M020 Lip Protecting TITANIUM DIOXIDE, ZINC OXIDE JOHANNA'S SKIN CARE 3544b8f2-2651-4c01-e063-6394a90ae53d 2025-12-12 Exact identifier application number: M020 Tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE JOHANNA'S SKIN CARE 3544faa1-ebdf-5dbd-e063-6394a90a7631 2025-12-12 Exact identifier application number: M020 Replenishing Daily Protection Tinted ZINC OXIDE SOLUTIONS SKIN CARE LLC 40323dfa-29e4-1464-e063-6294a90aa65c 2025-12-12 Warnings Exact identifier application number: M020 Zinc 20Percent SPF 40 ZINC OXIDE JOHANNA'S SKIN CARE 3545ed3e-b42f-d29d-e063-6394a90a8efe 2025-12-12 Exact identifier application number: M020 Replenishing Daily Protection Non-Tinted ZINC OXIDE SOLUTIONS SKIN CARE LLC 40332cf3-e4e5-0c00-e063-6394a90a683d 2025-12-12 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