Home NDC 72104-362 Nova Bright Skin SPF 30
Product NDC 72104-362
11-digit product format 721040362
Labeler code 72104
Product ID 72104-362_5a9283f7-8be2-4f48-bf51-bcfadb76ad7b
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Homosalate, Octisalate, Oxybenzone, Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler Innovation Brands Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-09-01
Substance OCTINOXATE; HOMOSALATE; OCTISALATE; OXYBENZONE; AVOBENZONE
Active strength 7.4; 6.2; 5; 3.1; 1.5 g/100g; g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 28 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 2025-04-01 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 72104-362-55 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72104-362-81 D Discontinued by firm 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 72104-362-55 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72104-362-81 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 72104-362-81 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 72104-362-81 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 72104-362-81 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 72104-362-81 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 72104-362-81 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Nova Bright Skin SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.4 g/100g HOMOSALATE 6.2 g/100g OCTISALATE 5 g/100g OXYBENZONE 3.1 g/100g AVOBENZONE 1.5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72104-362-55 Nova Bright Skin SPF 30 1 in 1 CARTON CREAM 1 4 72104-362-55 Nova Bright Skin SPF 30 55 g in 1 JAR CREAM 55 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72104-362 NOVA BRIGHT SKIN SPF 30 (OCTINOXATE, HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [LIONESSE USA, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20220811_1c201147-7a54-41b5-bdf0-394e3d7efc0c.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 148 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineral SPF 40, Tinted TITANIUM DIOXIDE, ZINC OXIDE Acne Specialists LLC 2fb14c4f-a435-aa6e-e063-6394a90a7d8d 2025-12-08 Warnings Exact identifier application number: M020 Mineral Sunscreen SPF 40 Non-Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc4f701-eea2-7913-e063-6294a90a8693 2025-12-08 Warnings Exact identifier application number: M020 Mineral Sunscreen SPF 40 Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc55e8c-41d6-15cc-e063-6394a90ac543 2025-12-08 Warnings Exact identifier application number: M020 Zinc Oxide SPF 40 Tinted ZINC OXIDE Skin Restoration Aesthetics 2fc60a39-789b-3d11-e063-6294a90a9abf 2025-12-08 Warnings Exact identifier application number: M020 Zinc Oxide SPF 40 Non-Tinted ZINC OXIDE Skin Restoration Aesthetics 2fc68041-acfe-8db6-e063-6294a90ad8ba 2025-12-08 Warnings Exact identifier application number: M020 Daily Tinted Mineral SPF TITANIUM DIOXIDE, ZINC OXIDE Skin Restoration Aesthetics 2fc6e168-b2c1-bf9d-e063-6394a90aade7 2025-12-08 Warnings Exact identifier application number: M020 Ultra Solar Shield non-tinted moisturizing mineral SPF 40 ZINC OXIDE Joyce Kelly Enterprises 365bdf7a-c034-beef-e063-6394a90a4dd7 2025-12-08 Exact identifier application number: M020 UV Shade tinted matte mineral SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Joyce Kelly Enterprises 365b3a1e-8410-da06-e063-6294a90a462f 2025-12-08 Exact identifier application number: M020 Solar Shield non-tinted matte mineral SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Joyce Kelly Enterprises 365b68a0-0f89-0f43-e063-6294a90a5eee 2025-12-08 Exact identifier application number: M020 Ultra UV Shade tinted moisturizing mineral SPF 40 ZINC OXIDE Joyce Kelly Enterprises 365ba78a-b7df-a31f-e063-6394a90a1673 2025-12-08 Exact identifier application number: M020 Mineral Sunscreen tinted TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3000a0a7-2b51-b832-e063-6294a90a4a08 2025-12-08 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3001028b-bb36-04ec-e063-6294a90a1e49 2025-12-08 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 3001aa3a-cc8b-6ad4-e063-6394a90a223f 2025-12-08 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Face 5, LLC 300268ff-f9ef-1006-e063-6294a90a5fdf 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF 40 Lightly Tinted ZINC OXIDE Face 5, LLC 3001ef4f-4cbb-8931-e063-6394a90a5cef 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF40 Non-Tinted ZINC OXIDE Face 5, LLC 300218c9-65cf-d984-e063-6294a90a1517 2025-12-08 Warnings Exact identifier application number: M020 Illuminating Daily SPF 40 Lightly Tinted ZINC OXIDE Face 5, LLC 300303e7-ef89-7449-e063-6294a90ac811 2025-12-08 Warnings Exact identifier application number: M020 Clear Path Tinted Facial Sunscreen TITANIUM DIOXIDE, ZINC OXIDE LULUS SPA BOUTIQUE 37657755-fa82-88a0-e063-6394a90ade47 2025-12-08 Exact identifier application number: M020 Tinted Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Dermacare 376468ce-8d9b-b672-e063-6294a90a0bd1 2025-12-08 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Dermacare 37643884-f186-fb54-e063-6394a90a450f 2025-12-08 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 72104-362-55 72104036255 1 JAR in 1 CARTON (72104-362-55) / 55 g in 1 JAR 1 jar 2021-01-27 0000-00-00 No No Current