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 19 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineral Sunscreen SPF 50 MINERAL SUNSCREEN ALAINA HEALTHCARE PRIVATE LIMITED 7e036f9f-b26d-4f11-911c-c1fa854edb0f 2026-06-17 Warnings Exact identifier application number: M020 Not there spf broad spectrum spf40 moisturizer AVOBENZONE 3% ,HOMOSALATE 10% ,OCTISALATE 5% ,OCTOCRYLENE 8% ,ZINC OXIDE 4% Foshan Sugar Max Cosmetics CO.,Ltd 546f0474-4102-26d0-e063-6394a90a388b 2026-06-17 Warnings Exact identifier application number: M020 Ultra Violette Velvet Screen Blurring Mineral Skinscreen Broad Spectrum SPF 40 ZINC OXIDE Grace and Fire USA Inc. 52d4b1c1-7431-4f8c-e063-6294a90ad482 2026-06-17 Warnings Exact identifier application number: M020 EVIL GOODS TALLOW SUNSCREEN SPF30 ZINC OXIDE Moes Group LLC 54751f23-5723-0407-e063-6294a90a4a96 2026-06-17 Warnings Exact identifier application number: M020 Amber Sunglaze Sheer Body Mist Sunscreen SPF30 AVOBENZONE, OCTISALATE, OCTOCRYLENE Koco Life LLC 5478fb36-e972-f824-e063-6294a90a567f 2026-06-17 Warnings Exact identifier application number: M020 Elaine Sterling Hydrating Sunscreen ZINC OXIDE Elaine Sterling Enterprises 5479e862-aca5-7541-e063-6394a90ad0c5 2026-06-17 Warnings Exact identifier application number: M020 No7 Restore and Renew Multi Action Day Cream Sunscreen Broad Spectrum SPF 25 AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE BCM Cosmetique SAS 545aa56a-ed07-acd6-e063-6394a90ae0c7 2026-06-16 Warnings Exact identifier application number: M020 MAYBELLINE NEW YORK FIT ME DEWY PLUS SMOOTH FOUNDATION SPF 18 SUNSCREEN OCTISALATE LOreal USA Products Inc 3b99ab06-ba4c-4ddd-a057-60028eedd67d 2026-06-16 Warnings Exact identifier application number: M020 TERRA LOTUS SPF 50 ORGANIC TALLOW SUNSCREEN ZINCOXIDE Moes Group LLC 54617bf2-1d8d-531e-e063-6294a90a7080 2026-06-16 Warnings Exact identifier application number: M020 Daily Defence Mineral Sunscreen SPF 50 Fragrance Free ZINC OXIDE Ultraceuticals Pty Ltd 5461ee82-0297-ce22-e063-6294a90a729b 2026-06-16 Warnings Exact identifier application number: M020 GlowBiotics Tinted Sunscreen SPF 30 ZINC OXIDE Rum Brands, LLC 544dba29-4785-4ab6-e063-6394a90a17b3 2026-06-16 Warnings Exact identifier application number: M020 Societe Prime and Defend ZINC OXIDE SUNSCREEN Societe Clinical Skincare 5439bd31-5ee1-9bca-e063-6394a90a748c 2026-06-16 Warnings Exact identifier application number: M020 Societe CoverShield Tinted SPF ZINC OXIDE Societe Clinical Skincare 545efbc4-82d4-f126-e063-6294a90a9710 2026-06-16 Warnings Exact identifier application number: M020 TITAN TALLOW SPF 50 ORGANIC TALLOW SUNSCREEN ZINC OXIDE Moes Group LLC 546b0702-a3cc-fd6f-e063-6394a90af849 2026-06-16 Warnings Exact identifier application number: M020 365 WHOLE FOODS MARKET MINERAL SPF 30 ZINC OXIDE Whole Foods Market, Inc. 5ce712d6-cafd-4a80-9f8c-2149fdebff54 2026-06-16 Warnings Exact identifier application number: M020 365 WHOLE FOODS MARKET MINERAL SPF 50 ZINC OXIDE Whole Foods Market, Inc. 1f8387be-d871-435b-baef-e537c67a510a 2026-06-15 Warnings Exact identifier application number: M020 365 WHOLE FOODS MARKET SUNSCREEN CLEAR COCONUT VANILLA SPF 50 OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND HOMOSALATE Whole Foods Market, Inc. 82771f22-0197-40ba-97d2-2386152790ed 2026-06-15 Warnings Exact identifier application number: M020 365 WHOLE FOODS MARKET SUNSCREEN CLEAR COCONUT VANILLA SPF 30 OCTOCRYLENE, OCTISALATE, AND AVOBENZONE Whole Foods Market, Inc. 1c31f466-6a0d-46ce-9346-d2a0eb46c8d0 2026-06-15 Warnings Exact identifier application number: M020 Shield by HEALTHY SKIN LAB MD SUNSCREEN TITANIUM DIOXIDE, ZINC OXIDE HEALTHY SKIN LAB LIMITED 6838b754-9915-48ff-af35-5338dbd06ac4 2026-06-15 Warnings Exact identifier application number: M020 Solvyn Mineral Sunscreen SPF 50 ZINC OXIDE Solvyn Skin LLC b0a8d028-87d2-4339-8879-c62cbf8415f2 2026-06-15 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