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 184 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PUR 4-in-1 Skin Tint MN3 ZINC OXIDE PUR Minerals 3f06df49-5ed2-44ca-e063-6294a90a1fda 2025-09-24 Warnings Exact identifier application number: M020 PUR 4-in-1 Skin Tint LN2 ZINC OXIDE PUR Minerals 3f069dfe-289d-8d3b-e063-6394a90a0496 2025-09-24 Warnings Exact identifier application number: M020 PUR 4-in-1 Skin Tint LG3 ZINC OXIDE PUR Minerals 3f06ec3e-fc15-9f7b-e063-6394a90a0733 2025-09-24 Warnings Exact identifier application number: M020 Volition Prismatic Luminizing Shield ZINC OXIDE Volition 1a633c24-b9d9-4732-e063-6294a90af4c0 2025-09-24 Warnings Exact identifier application number: M020 Alleyoop Sunsational Broad Spectrum ZINC OXIDE NewAlley Innovations Inc 248419c4-8044-402c-e063-6394a90a00f8 2025-09-24 Warnings Exact identifier application number: M020 Aloe Up SPF 30 coco-mango mist AVOBENZONE 3.0%, HOMOSALATE 7.5%, OCTISALATE 5.0% Aloe Up f7b2d4a2-3a0d-4239-b7e5-8de2f6ac2e92 2025-09-24 Warnings Exact identifier application number: M020 pavise Dynamic Age Defense ZINC OXIDE B.A.I BIOSCIENCES, INC f4e9f95c-6b1e-d5f7-e053-2a95a90a93ce 2025-09-24 Warnings Exact identifier application number: M020 Aloe Up SPF 50 coco-mango mist AVOBENZONE 3.0%, HOMOSALATE 10.0%, OCTISALATE 5.0% Aloe Up d535b711-c54e-4447-9907-ca9d829d1319 2025-09-24 Warnings Exact identifier application number: M020 ESPOIR WATER SPLASH SUN SERUM HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE ESPOIR Corporation 1c4e7ba2-05e8-f949-e063-6394a90a699d 2025-09-23 Warnings Exact identifier application number: M020 Banana Boat ZINC OXIDE Edgewell Personal Care Brands LLC 1d11c3d0-5f4e-0ed0-e063-6294a90abc75 2025-09-23 Warnings Exact identifier application number: M020 Dewscreen Daily Hydrator and Primer SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Supergoop LLC 3f7c84e3-0e4f-b7e9-e063-6294a90a1295 2025-09-23 Warnings Exact identifier application number: M020 Sun Bum Daily Gel Gel Sunscreen Moisturizer Broad Spectrum SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Sun Bum, LLC 15d8574d-94bb-4842-e063-6394a90a15e6 2025-09-23 Warnings Exact identifier application number: M020 Sun Bum Daily Body AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Sun Bum, LLC 15da0cb1-e695-cec3-e063-6394a90a1afa 2025-09-23 Warnings Exact identifier application number: M020 Sun Bum Daily Face Liquid Sunscreen Moisturizer Broad Spectrum SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Sun Bum, LLC 15daac41-54b6-096d-e063-6294a90a0736 2025-09-23 Warnings Exact identifier application number: M020 Mtn. Bum by Sun Bum and Mcfetridge Mineral Sunscreen Face Stick SPF 50 ZINC OXIDE Sun Bum, LLC 3f8101b1-297d-2ad8-e063-6294a90a9cff 2025-09-23 Warnings Exact identifier application number: M020 Sun Bum Daily Glow Tinted Sunscreen Moisturizer Broad Spectrum SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE Sun Bum, LLC 20c48752-3ad9-5993-e063-6294a90ae1b0 2025-09-23 Warnings Exact identifier application number: M020 CVS SPF 60 Face Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CVS 26d1b568-ad9c-80d7-e063-6394a90a2cbf 2025-09-21 Warnings Exact identifier application number: M020 Radiant Shield Tinted Mineral Sunscreen SPF 40 ZINC OXIDE CosMedical Technologies, LLC f229b928-49fd-4e02-99c1-b2cd9166894f 2025-09-19 Warnings Exact identifier application number: M020 EquateDaytimeFaceLotion EQUATE DAYTIME FACE LOTION WITH SUNSCREEN, SPF 30, 3 OZ Walmart Inc. 2efc7087-f4ad-2f2e-e063-6394a90a1302 2025-09-18 Warnings Exact identifier application number: M020 ERBORIAN CC RED CORRECT ERBORIAN CC RED CORRECT SPF 25- OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE CREAM Kolmask Co., Ld. 09ca2d4b-e0c2-9961-e063-6394a90aa82e 2025-09-18 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