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 221 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HEB SPF 50 Mangonada Scented Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B 3147ef18-9029-6d5b-e063-6394a90acee0 2025-03-26 Warnings Exact identifier application number: M020 HEB SPF 50 Mexican Vanilla Scented Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B 31487bad-a756-9050-e063-6394a90acacc 2025-03-26 Warnings Exact identifier application number: M020 TRADER JOES DAILY FACIAL MINERAL SUNSCREEN SPF 40 ZINC OXIDE Trader Joe's Company 3148c00f-21bb-c05f-e063-6394a90af0e8 2025-03-26 Warnings Exact identifier application number: M020 HEB SPF 50 Chamomile and Lavender Scented Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B 314b8147-fe7a-0698-e063-6394a90a872c 2025-03-26 Warnings Exact identifier application number: M020 HEB SPF 50 Shine Sunscreen with Vitamin C Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B 314bcf42-ca01-0fa5-e063-6294a90a5fc8 2025-03-26 Warnings Exact identifier application number: M020 Superactive Moisturizer SPF 50 Hydrating SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Murad, LLC 1e5d494b-dccf-4ba1-89de-0bb4ba5b8d38 2025-03-26 Warnings Exact identifier application number: M020 Superactive Moisturizer SPF 50 Wrinkle Fighting SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE Murad, LLC ac6163fb-dbc1-432f-a590-86d31c93b29b 2025-03-26 Warnings Exact identifier application number: M020 it cosmetics Your Skin But Better CC Plus Color Correcting Broad Spectrum SPF 50 Plus Sunscreen Full Coverage Deep FairLight Neutral Tan Rich Honey LightMedium and Neutral Medium TITANIUM DIOXIDE AND ZINC OXIDE IT COSMETICS, LLC e17dc640-30e9-441b-a212-ef1508af7944 2025-03-25 Warnings Exact identifier application number: M020 Lip Balm SPF15 Vanilla LIP BALM SPF15 VANILLA LS Promotions Inc 312d0dc5-3933-ecfe-e063-6294a90a9b66 2025-03-25 Warnings Exact identifier application number: M020 Lip Balm SPF15 Blueberry Cobbler LIP BALM SPF15 BLUEBERRY COBBLER LS Promotions Inc 312fb7b0-86a9-ca88-e063-6294a90a76c8 2025-03-25 Warnings Exact identifier application number: M020 Lip Balm SPF15 Peppermint LIP BALM SPF15 PEPPERMINT LS Promotions Inc 3130be1c-0167-2389-e063-6394a90aa61d 2025-03-25 Warnings Exact identifier application number: M020 Drs. pharmacy sunscreen SPF 30 SUNSCREEN SPF 30 OL PHARMA TECH LLC. (Drs. Pharmacy) 052dea5d-a775-8dc2-e063-6294a90a4f19 2025-03-25 Warnings Exact identifier application number: M020 Drs. pharmacy sunscreen SPF 50 SUNSCREEN SPF 50 OL PHARMA TECH LLC. (Drs. Pharmacy) 0def5c19-b088-2ffb-e063-6394a90aa109 2025-03-25 Warnings Exact identifier application number: M020 Drs. pharmacy sunscreen SPF 70 SUNSCREEN SPF 70 OL PHARMA TECH LLC. (Drs. Pharmacy) 0def6fa1-b028-fad5-e063-6394a90a1913 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84521 ZINC OXIDE e.l.f. Cosmetics, Inc. 31329426-d952-ee5d-e063-6294a90a55f4 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84520 ZINC OXIDE e.l.f. Cosmetics, Inc. 31328845-9a67-d237-e063-6294a90a2a7f 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84519 ZINC OXIDE e.l.f. Cosmetics, Inc. 31327ea3-affd-ca13-e063-6294a90a7238 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84517 ZINC OXIDE e.l.f. Cosmetics, Inc. 3132641a-e593-a9e8-e063-6294a90acc80 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF50 -84518 ZINC OXIDE e.l.f. Cosmetics, Inc. 3132669c-e104-ae1e-e063-6294a90aee7f 2025-03-25 Warnings Exact identifier application number: M020 Halo Glow Skin Tint SPF 50 84514 ZINC OXIDE e.l.f. Cosmetics, Inc. 31324410-3142-89e1-e063-6294a90a22ee 2025-03-25 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