Home NDC 43419-079 SULWHASOO PERFECTING CUSHION NO. 25
Product NDC 43419-079
11-digit product format 434190079
Labeler code 43419
Product ID 43419-079_440a35c1-f129-3c36-e063-6294a90a537d
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Amorepacific Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-15
Marketing end 2027-03-31
Substance OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 2.1; 1.245; 2.94 g/30g; g/30g; g/30g
NDC exclude flag No
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 SULWHASOO PERFECTING CUSHION NO. 25 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 2.1 g/30g TITANIUM DIOXIDE 1.245 g/30g ZINC OXIDE 2.94 g/30g
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 15FIX9V2JP Internal UNII lookup 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 43419-079-31 SULWHASOO PERFECTING CUSHION NO. 25 15 g in 1 CONTAINER LOTION 15 10 43419-079-31 SULWHASOO PERFECTING CUSHION NO. 25 2 in 1 CARTON LOTION 2 10 43419-079-39 SULWHASOO PERFECTING CUSHION NO. 25 15 g in 1 CONTAINER LOTION 15 10 43419-079-39 SULWHASOO PERFECTING CUSHION NO. 25 2 in 1 CARTON LOTION 2 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43419-079 SULWHASOO PERFECTING CUSHION NO. 21 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 27 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 31 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 33 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 15 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 17 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 23 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 37 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 11 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION SULWHASOO PERFECTING CUSHION NO. 25 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION [AMOREPACIFIC CORPORATION] 9 Current NDC, Legacy NDC, 4 package rows 20241012_8d420e4b-c778-3ed4-e053-2995a90a59a9.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43419-079-31 43419007931 2 CONTAINER in 1 CARTON (43419-079-31) / 15 g in 1 CONTAINER 2 container 2019-07-15 2027-03-31 No No Current 43419-079-39 43419007939 2 CONTAINER in 1 CARTON (43419-079-39) > 15 g in 1 CONTAINER 2 container 2019-12-09 2021-12-02 No No Current