Home NDC 76340-3001-1 Dr.eslee Sun Matte
Product NDC 76340-3001
Requested package NDC 76340-3001-1
11-digit product format 763403001
Labeler code 76340
Product ID 76340-3001_6304bca3-e4a5-c11c-e053-2a91aa0a0dee
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE
Dosage form LIQUID
Route TOPICAL
Labeler Ajou Medics Co., Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2011-08-10
Marketing end 0000-00-00
Substance OCTINOXATE
Active strength 8 g/100g
NDC exclude flag No
Listing certified through 2020-12-31
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 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded OCTINOXATE ACTIVE INGREDIENT 4Y5P7MUD51 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 OCTINOXATE ACTIVE MOIETY 4Y5P7MUD51 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 ALUMINUM HYDROXIDE INACTIVE INGREDIENT 5QB0T2IUN0 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 BIOSACCHARIDE GUM-1 INACTIVE INGREDIENT BB4PU4V09H DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 BUTYLENE GLYCOL INACTIVE INGREDIENT 3XUS85K0RA DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 C12-16 ALCOHOLS INACTIVE INGREDIENT S4827SZE3L DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 CYCLOMETHICONE INACTIVE INGREDIENT NMQ347994Z DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 ENZACAMENE INACTIVE INGREDIENT 8I3XWY40L9 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 FARNESOL INACTIVE INGREDIENT EB41QIU6JL DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 GLYCERYL MONOSTEARATE INACTIVE INGREDIENT 230OU9XXE4 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 HYALURONATE SODIUM INACTIVE INGREDIENT YSE9PPT4TH DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 HYDROGENATED POLYDECENE (550 MW) INACTIVE INGREDIENT U333RI6EB7 DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 OCTOCRYLENE INACTIVE INGREDIENT 5A68WGF6WM DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 PEG-100 STEARATE INACTIVE INGREDIENT YD01N1999R DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 PHENOXYETHANOL INACTIVE INGREDIENT HIE492ZZ3T DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 POLYHYDROXYSTEARIC ACID (2300 MW) INACTIVE INGREDIENT YXH47AOU0F DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 SALICYLIC ACID INACTIVE INGREDIENT O414PZ4LPZ DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 SORBITAN MONOSTEARATE INACTIVE INGREDIENT NVZ4I0H58X DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1 ZINC SULFATE INACTIVE INGREDIENT 89DS0H96TB DR.ESLEE SUN MATTE (OCTINOXATE) LIQUID [AJOU MEDICS CO., LTD] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76340-3001-1 76340300101 60 g in 1 TUBE (76340-3001-1) 60 g 2016-01-01 0000-00-00 No No Current