Home NDC 69494-302 Eryfotona Actinica Ultralight Emulsion
Product NDC 69494-302
11-digit product format 694940302
Labeler code 69494
Product ID 69494-302_a2e2bbf6-ebd4-4c22-bdf2-49652583d714
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form EMULSION
Route TOPICAL
Labeler ISDIN Corp
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-08-17
Substance ZINC OXIDE
Active strength 11 g/100mL
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Eryfotona Actinica Ultralight Emulsion
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 11 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69494-302-10 Eryfotona Actinica Ultralight Emulsion 1 in 1 CARTON EMULSION 1 11 69494-302-10 Eryfotona Actinica Ultralight Emulsion 10 mL in 1 BOTTLE, PLASTIC EMULSION 10 11 69494-302-11 Eryfotona Actinica Ultralight Emulsion 2 mL in 1 TUBE EMULSION 2 11 69494-302-11 Eryfotona Actinica Ultralight Emulsion 12 in 1 CARTON EMULSION 12 11 69494-302-12 Eryfotona Actinica Ultralight Emulsion 1 in 1 CARTON EMULSION 1 11 69494-302-12 Eryfotona Actinica Ultralight Emulsion 2 mL in 1 BOTTLE, PLASTIC EMULSION 2 11 69494-302-13 Eryfotona Actinica Ultralight Emulsion 1 in 1 CARTON EMULSION 1 11 69494-302-13 Eryfotona Actinica Ultralight Emulsion 50 mL in 1 BOTTLE, PLASTIC EMULSION 50 11 69494-302-14 Eryfotona Actinica Ultralight Emulsion 12 in 1 CARTON EMULSION 12 11 69494-302-14 Eryfotona Actinica Ultralight Emulsion 4 mL in 1 TUBE EMULSION 4 11 69494-302-15 Eryfotona Actinica Ultralight Emulsion 4 mL in 1 TUBE EMULSION 4 11 69494-302-15 Eryfotona Actinica Ultralight Emulsion 1 in 1 PACKET EMULSION 1 11 69494-302-30 Eryfotona Actinica Ultralight Emulsion 1 in 1 CARTON EMULSION 1 11 69494-302-30 Eryfotona Actinica Ultralight Emulsion 100 mL in 1 BOTTLE, PLASTIC EMULSION 100 11
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69494-302 ERYFOTONA ACTINICA ULTRALIGHT EMULSION (SUNSCREEN) EMULSION [ISDIN CORP] 11 Current NDC, Legacy NDC, 14 package rows 20241121_1d4b88d3-bee9-102c-e054-00144ff8d46c.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 87 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dr Loretta Universal Glow Daily Defense SPF 40 ZINC OXIDE Dr. Loretta, LLC 1208d0f8-bb12-4574-b70e-3a76b11a64c7 2026-01-07 Warnings Exact identifier application number: M020 Neutrogena Ultra Sheer Face Sunscreen SPF 60 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE KDC/One Development Corporation, Inc. 259f3fe3-2967-6c05-e063-6394a90a9e45 2026-01-07 Warnings Exact identifier application number: M020 Hawaiian Blend Extreme Zinc SPF 30 ZINC OXIDE, TITANIUM DIOXIDE The Islander Group 4084dd98-357f-4011-b0d4-db6536d2931f 2026-01-07 Warnings Exact identifier application number: M020 Hawaiian Blend Extreme Zinc SPF 50 ZINC OXIDE, TITANIUM DIOXIDE The Islander Group 9b4acc5e-fdaf-4fcb-83a9-69e430dd43de 2026-01-07 Warnings Exact identifier application number: M020 Hawaiian Blend Sensitive Zinc SPF 50 ZINC OXIDE, TITANIUM DIOXIDE The Islander Group b42261c5-fa6e-4bb3-93c0-97032ab9f716 2026-01-07 Warnings Exact identifier application number: M020 CabanaMilk Mineral Barrier Fluid SPF 50 ZINC OXIDE NAKED SUNDAYS PTY LTD 47d0fe4d-ad21-1004-e063-6394a90a9c19 2026-01-07 Warnings Exact identifier application number: M020 CENTELLA RELIEF SOOTHING SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE IUNIK Co., Ltd. 47d170e3-dd76-d413-e063-6294a90ae8e4 2026-01-07 Warnings Exact identifier application number: M020 Round Lab Birch Juice Mild-Up UVLOCK Sunscreen SPF50 Broad Spectrum ZINC OXIDE SEORIN COMPANY Co., Ltd. 1e7cc417-3c57-c87c-e063-6394a90a670b 2026-01-07 Warnings Exact identifier application number: M020 Proactiv Clear Skin SPF 30 AVOBENZONE, OCTISALATE, AND OCTOCRYLENE Alchemee, LLC b0aa7ff0-f712-486f-aaaf-f88fed3b5cd1 2026-01-07 Warnings Exact identifier application number: M020 Daily Hydrating Mineral Body Sunscreen Broad Spectrum SPF 30 Sunscreen ZINC OXIDE Oak Essentials, LLC 47d37f44-10b2-214f-e063-6294a90a5abc 2026-01-07 Warnings Exact identifier application number: M020 PLUMSCREEN SPF 31 ZINC OXIDE Le Prunier Farms, Inc. e20eb996-2b64-6bd0-e053-2a95a90a4f92 2026-01-07 Warnings Exact identifier application number: M020 BETA-GLUCAN MILD SUNSCREEN TITANIUM DIOXIDE, ZINC OXIDE IUNIK Co., Ltd 47d6ad8b-1081-ee21-e063-6294a90a0e63 2026-01-07 Warnings Exact identifier application number: M020 Koobarra Mineral Face Sunscreen SPF 50 ZINC OXIDE SUNSCREEN VEGANIC SKN LIMITED 37cf8143-99f2-cca5-e063-6394a90a19a8 2026-01-07 Warnings Exact identifier application number: M020 Solar Swipe Mineral Sunscreen SPF50 SOLAR SWIPE MINERAL SUNSCREEN SPF50 Guangzhou Fantesy Biotechnology Co.,Ltd 47d75d61-5295-3eab-e063-6394a90a01c1 2026-01-07 Warnings Exact identifier application number: M020 LUXURY SUN RITUAL PORE SMOOTHING SPF 30 SUNSCREEN ZINC OXIDE JANE STREET LLC dbdd3e6a-f09d-90cf-e053-2a95a90a98a0 2026-01-07 Warnings Exact identifier application number: M020 RENEWALUXE SPF 50 Sunscreen RENEWALUXE SPF 50 SUNSCREEN Guangzhou Fantesy Biotechnology Co.,Ltd 1bc29960-5e73-e8ab-e063-6294a90a3f80 2026-01-06 Warnings Exact identifier application number: M020 ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN SPF50 Wild Child Laboratories PTY Ltd 2767ba3e-7434-d474-e063-6294a90aa4ff 2026-01-06 Warnings Exact identifier application number: M020 ULTRA VIOLETTE SPF ON THE GLOW Duo Pack Kit SPF 50 Grace And Fire USA Inc. 47b7da8a-ea89-1402-e063-6294a90a23f9 2026-01-06 Warnings Exact identifier application number: M020 Hawaiian Blend Essential Zinc SPF 30 ZINC OXIDE, TITANIUM DIOXIDE The Islander Group 5a6e622f-2c00-406a-8860-d7081656f597 2026-01-06 Warnings Exact identifier application number: M020 SHISEIDO SYNCHRO SKIN LASTING Liquid FOUNDATION Neutral 5 OCTINOXATE AND TITANIUM DIOXIDE SHISEIDO AMERICAS CORPORATION 66c22f17-5418-42ff-97b2-33fa10f5eac3 2026-01-06 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 69494-302-10 69494030210 10 g in 1 BOTTLE (69494-302-10) 10 g 2016-02-24 0000-00-00 No No Current 69494-302-11 69494030211 12 TUBE in 1 CARTON (69494-302-11) / 2 mL in 1 TUBE 12 tube 2023-12-18 No No Current 69494-302-12 69494030212 1 BOTTLE, PLASTIC in 1 CARTON (69494-302-12) / 2 mL in 1 BOTTLE, PLASTIC 2019-11-01 0000-00-00 Yes No Current 69494-302-13 69494030213 1 BOTTLE, PLASTIC in 1 CARTON (69494-302-13) / 50 mL in 1 BOTTLE, PLASTIC 2023-05-01 No No Current 69494-302-14 69494030214 12 TUBE in 1 CARTON (69494-302-14) / 4 mL in 1 TUBE 12 tube 2023-10-30 No No Current 69494-302-15 69494030215 1 TUBE in 1 PACKET (69494-302-15) / 4 mL in 1 TUBE 1 tube 2024-07-01 No No Current 69494-302-30 69494030230 1 BOTTLE, PLASTIC in 1 CARTON (69494-302-30) / 100 mL in 1 BOTTLE, PLASTIC 2019-11-01 0000-00-00 No No Current