Home NDC 58414-0019 NeoStrata Enlighten Skin Brightener
Product NDC 58414-0019
11-digit product format 584140019
Labeler code 58414
Product ID 58414-0019_59e15d1b-73fa-37e9-e063-6394a90a5d62
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Octisalate, and Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler NeoStrata Company Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-12-01
Substance OCTINOXATE; OCTISALATE; AVOBENZONE
Active strength 75; 50; 30 mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 8 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 2025-01-11 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 58414-0019-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 58414-0019-1 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…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 58414-0019-1 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 58414-0019-1 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 NeoStrata Enlighten Skin Brightener
Brand name suffix with Sunscreen Broad Spectrum SPF 35
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/g OCTISALATE 50 mg/g AVOBENZONE 30 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup
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 58414-0019-1 NeoStrata Enlighten Skin Brightenerwith Sunscreen Broad Spectrum SPF 35 40 g in 1 TUBE CREAM 40 4 58414-0019-1 NeoStrata Enlighten Skin Brightenerwith Sunscreen Broad Spectrum SPF 35 1 in 1 CARTON CREAM 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58414-0019 NEOSTRATA ENLIGHTEN SKIN BRIGHTENER WITH SUNSCREEN BROAD SPECTRUM SPF 35 (OCTINOXATE, OCTISALATE, AND AVOBENZONE) CREAM [NEOSTRATA COMPANY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250112_ed495f18-2f8e-4991-b797-82e9f6fc7acb.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 46 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Arizona Sun Sunscreen SPF 30 SUNSCREEN Arizona Sun Products 10e276e4-81f1-9429-e063-6394a90a800d 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen SPF 8 SUNSCREEN Arizona Sun Products 106a9608-f7a4-0f8c-e063-6394a90a26ab 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Bikerblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fced72-39f9-f3a3-e063-6294a90a8b73 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Golfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fc2a82-260c-7cd3-e063-6394a90af2c1 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Cycleblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fd9aa5-dbd6-e5a7-e063-6394a90a3eac 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Golfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fc93a7-f5be-965d-e063-6394a90ab335 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Bikerblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fd1661-1b91-b65b-e063-6394a90af89b 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Lipkist Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fbcb81-2735-53c8-e063-6394a90ab0fa 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Products Cycleblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fd8776-99f8-e5a4-e063-6394a90a2033 2026-04-09 Warnings Exact identifier application number: M020 uLOOK Sunscreen SPF 50 SUNSCREEN HAMEX GLOBAL COSMETICS LLC 4e05588c-486b-60e0-e063-6294a90af457 2026-04-09 Warnings Exact identifier application number: M020 Pro-Tect Sports Sunscreen SPF 20 MERADIMATE, OCTINOXATE, OCTISALATE, OXYBENZONE ABBE Laboratories, Inc. 35869e8d-8e48-4b22-8af3-6964fe8ac182 2026-04-09 Warnings Exact identifier application number: M020 Sunright 50 AVOBENZONE, HOMOSALATE, AND OCTINOXATE NSE Products, Inc. b1b76481-da23-427f-9b34-b987019fa532 2026-04-09 Warnings Exact identifier application number: M020 ThinkBaby SPF 30 ZINC OXIDE thinkOperations,LLC 06862b00-c937-41af-ab5d-cea34160d035 2026-04-09 Warnings Exact identifier application number: M020 Nutricentials Day Dream Protective HOMOSALATE, OCTISALATE, AVOBENZONE, AND OCTOCRYLENE NSE Products, Inc. 4a376e93-85e8-40a5-8641-d3e3d11fdeea 2026-04-08 Warnings Exact identifier application number: M020 AGE20S SUNSCREEN DUO ZINC OXIDE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Aekyung Industrial Co., Ltd. 4eef11cd-85a1-0e44-e063-6394a90a5d44 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena MINERAL UV TINT FACE DEEP SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc. 4ef430e8-cdc8-2897-e063-6394a90a3ac7 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena MINERAL UV TINT FACE LIGHT SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc. 4ef4a822-a7ab-b374-e063-6394a90a8508 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena MINERAL UV TINT FACE MEDIUM SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc. 4ef4d44e-3421-535f-e063-6294a90a2fea 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 and Neutrogena Collagen Bank Moisturizer AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Acupac Packaging, Inc. 4ef5baf7-00b1-97aa-e063-6294a90aab9c 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena Mineral Ultra Sheer Face SPF 70 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc. 4ef5dcd4-b2d0-bcd1-e063-6294a90a871f 2026-04-08 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 58414-0019-1 58414001901 1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE 1 tube 2018-12-01 0000-00-00 No No Current