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 241 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sheglam Dew and Done Skin Tint with SPF 20 Warm Vanilla ZINC OXIDE EVER FAME PTE. LTD. 2acf9020-c779-31c2-e063-6294a90a1ab5 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Eucalyptus Mint SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad009bc-29ce-0ba6-e063-6294a90a7580 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Bing Cherry SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad07286-f8af-7a9f-e063-6394a90a6a24 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Vanilla Bean SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad0db95-a283-3c91-e063-6294a90ae523 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Strawberry Breeze SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad129b7-4ecd-a967-e063-6294a90ad8c4 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Citrus Blast SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad18f4b-4251-be82-e063-6394a90acac5 2025-01-03 Warnings Exact identifier application number: M020 Earths Daughter Creamy Coconut SPF 15 Broad Spectrum Sunscreen Lip Balm AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Earth's Daughter 2ad1bb50-869e-8122-e063-6294a90ac724 2025-01-03 Warnings Exact identifier application number: M020 Glow Baby Brightening Setting Mist SPF 45 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Pacifica Beauty, LLC f2f53cf9-3717-07ff-e053-2a95a90a03fb 2025-01-03 Warnings Exact identifier application number: M020 Future Youth Daily Turnaround Hydrating Moisturizer SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE Pacifica Beauty, LLC 0324275f-13bc-e7b8-e063-6294a90a6902 2025-01-03 Warnings Exact identifier application number: M020 Glow Baby Super Lit SPF 30 ZINC OXIDE Pacifica Beauty, LLC f3d3eee2-a5d9-113b-e053-2995a90a7057 2025-01-03 Warnings Exact identifier application number: M020 Kind Tint SPF 30 ZINC OXIDE Pacifica Beauty, LLC f421cbf7-cfae-5eae-e053-2995a90ab35c 2025-01-03 Warnings Exact identifier application number: M020 Vegan Collagen Every Day SPF 30 AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTYL SALICYLATE Pacifica Beauty, LLC f449da32-5ade-2c78-e053-2a95a90a27a1 2025-01-03 Warnings Exact identifier application number: M020 Members Mark SPF 50 Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Sam's West Inc 2b354ab6-f241-676f-e063-6394a90a5893 2025-01-03 Warnings Exact identifier application number: M020 Vanilla Mint Lip Balm LIP BALM Casad Company Inc. 3214bff3-e133-43ca-946d-f4c5dd074760 2025-01-03 Warnings Exact identifier application number: M020 Vanilla Lip Balm LIP BALM Casad Company Inc. d27398d3-98b0-4f70-997e-6ed02559594f 2025-01-03 Warnings Exact identifier application number: M020 Cherry Lip Balm LIP BALM Casad Company Inc. b262645e-f069-420d-90ac-9eb4b82236d8 2025-01-03 Warnings Exact identifier application number: M020 Peppermint Lip Balm LIP BALM Casad Company Inc. 46a4b6d1-37e4-471d-a41b-57afe8bd9f2f 2025-01-03 Warnings Exact identifier application number: M020 Beeswax Lip Balm LIP BALM Casad Company Inc. 5301398d-82f8-495e-b3ec-0938eca16369 2025-01-03 Warnings Exact identifier application number: M020 Spearmint Lip Balm LIP BALM Casad Company Inc. ba9b5420-60b0-4528-9898-a0a5287a2aee 2025-01-03 Warnings Exact identifier application number: M020 Pomegranate Lip Balm LIP BALM Casad Company Inc. 4e943a8a-f627-4e28-bdd7-c2b63be5dca3 2025-01-03 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