Home NDC 61354-081 Cream
Product NDC 61354-081
11-digit product format 613540081
Labeler code 61354
Product ID 61354-081_e715df51-25f7-298a-e053-2a95a90a0464
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form LOTION
Route TOPICAL
Labeler Oxygen Development LLC
Application M020
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-08-25
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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 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 61354-081-01 Cream 100 mg in 1 TUBE LOTION 100 1 61354-081-01 Cream 1 in 1 CARTON LOTION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61354-081 CREAM (ZINC OXIDE, TITANIUM DIOXIDE) LOTION [OXYGEN DEVELOPMENT LLC] 1 Legacy NDC, 2 package rows 20220827_e715df51-25f6-298a-e053-2a95a90a0464.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 222 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Halo Glow Skin Tint SPF 50 84507 ZINC OXIDE e.l.f. Cosmetics, Inc. 31314118-0fd6-5549-e063-6394a90a9d1f 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF 50 84506 ZINC OXIDE e.l.f. Cosmetics, Inc. 313119be-c1f2-4cb0-e063-6294a90a03ca 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84516 ZINC OXIDE e.l.f. Cosmetics, Inc. 312dd439-5cc8-e034-e063-6394a90a5c76 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF 50 84504 ZINC OXIDE e.l.f. Cosmetics, Inc. 223efabb-d018-c337-e063-6394a90a5605 2025-03-25 Warnings Exact identifier application number: M020 IT Cosmetics Your Skin But Better CC Plus Color Correcting Full Coverage Antiaging Hydrating Serum Broad Spectrum SPF 50 Plus Clear Sunscreen HOMOSALATE, OCTISALATE AND OCTOCRYLENE IT COSMETICS, LLC 9f8786cc-bef6-4449-8f31-dfc08de77734 2025-03-25 Warnings Exact identifier application number: M020 it cosmetics Your Skin But Better CC Plus Oil Free Matte Poreless Finish Full Coverage Broad Spectrum SPF 40 Sunscreen All Shades TITANIUM DIOXIDE AND ZINC OXIDE IT COSMETICS, LLC b7d184fb-4a9a-4720-9b00-bf0caa257a8c 2025-03-25 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30cce5b1-ed41-5bf2-e063-6394a90aaf1d 2025-03-24 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30df95da-4868-1414-e063-6294a90acdac 2025-03-24 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30e1bd3c-6a0b-a8f8-e063-6394a90acfb7 2025-03-24 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30e1b4c9-0d77-b08a-e063-6394a90af683 2025-03-24 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30e1ff3f-0fd0-2880-e063-6294a90a462f 2025-03-24 Warnings Exact identifier application number: M020 KISS New York Tinted Moisturizer ZINC OXIDE IVY ENTERPRISES, INC. 30e25241-0d2b-8c04-e063-6294a90a44b9 2025-03-24 Warnings Exact identifier application number: M020 Walgreens SPF 50 Clear Complexion Face Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY 311ae6d6-d466-3f1d-e063-6294a90ab3dd 2025-03-24 Warnings Exact identifier application number: M020 DOMINAS DARK SPOT TINTED SUNSCREEN OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE LG H&H CO., LTD. 2b6140cf-7e34-1658-e063-6394a90a3271 2025-03-24 Warnings Exact identifier application number: M020 CVS Health SPF 70 Ultra Sheer AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CVS Pharmacy 311de9db-941c-5af9-e063-6294a90a3a13 2025-03-24 Warnings Exact identifier application number: M020 CVS Health SPF 70 Beach Guard Clear AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CVS Pharmacy 311e6378-5afa-d7eb-e063-6394a90a7728 2025-03-24 Warnings Exact identifier application number: M020 Naked Sundays Golden Glow Body Sunscreen SPF50 100ml NAKED SUNDAYS GOLDEN GLOW BODY SUNSCREEN SPF50 100ML NAKED SUNDAYS PTY LTD e182a39b-89b1-7756-e053-2a95a90ab619 2025-03-23 Warnings Exact identifier application number: M020 ANTIOXIDANT BODY SUNSCREEN CREME SPF50 BROAD SPECTRUM AVOBENZONE 30MG/G, HOMOSALATE 100MG/G, OCTOCRYLENE 100MG/G, OCTISALATE 50MG/G, NAKED SUNDAY PTY LTD eb7a84a8-3e25-9988-e053-2a95a90a58a9 2025-03-23 Warnings Exact identifier application number: M020 NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS Illuminating 40mL with Pink Algae SPF 50 TITANIUM OXIDE, ZINC OXIDE NAKED SUNDAYS PTY LTD 01273e8c-aef0-d800-e063-6294a90abd49 2025-03-23 Warnings Exact identifier application number: M020 NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS BRONZE 40mL with wild Rosella SPF 50 TITANIUM OXIDE, ZINC OXIDE NAKED SUNDAYS PTY LTD 01221d57-9eec-7e77-e063-6394a90a6042 2025-03-23 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 61354-081-01 61354008101 1 TUBE in 1 CARTON (61354-081-01) > 100 mg in 1 TUBE 1 tube 2022-08-25 0000-00-00 No No Current