Home NDC 69352-020 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID
Product NDC 69352-020
11-digit product format 693520020
Labeler code 69352
Product ID 69352-020_e4aa261a-6314-4e03-8803-b3a1879d4969
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Titanium Dioxide, Octisalate, Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler AMARTEINTERNATIONAL CO., LTD.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-10-01
Marketing end 0000-00-00
Substance OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE; ZINC OXIDE
Active strength 5 mg/70mL; mg/70mL; mg/70mL; mg/70mL
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record 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 · 26 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69352-020-01 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 69352-020-01 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 69352-020-01 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 69352-020-01 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 69352-020-01 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69352-020-01 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 69352-020-01 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 69352-020-01 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 69352-020-01 I Inactivated by FDA bd6a592717d7…303034d00443…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 69352-020-01 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 69352-020-01 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 69352-020-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 69352-020-01 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69352-020-01 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID 70 mL in 1 CARTON CREAM 70 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Octinoxate ACTIVE INGREDIENT 4Y5P7MUD51 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 Octisalate ACTIVE INGREDIENT 4X49Y0596W AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 Titanium Dioxide ACTIVE INGREDIENT 15FIX9V2JP AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 Zinc Oxide ACTIVE INGREDIENT SOI2LOH54Z AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 OCTINOXATE ACTIVE MOIETY 4Y5P7MUD51 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 OCTISALATE ACTIVE MOIETY 4X49Y0596W AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 TITANIUM DIOXIDE ACTIVE MOIETY 15FIX9V2JP AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69352-020 AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) CREAM [AMARTEINTERNATIONAL CO., LTD.] 3 Legacy NDC, 1 package rows 20240802_b2b7c425-6c60-41cf-adea-9c355b24a443.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 69352-020-01 69352002001 70 mL in 1 CARTON 70 ml Historical