Home NDC 69777-240 OrgaPlus Ultra Pure Sun EX
Product NDC 69777-240
11-digit product format 697770240
Labeler code 69777
Product ID 69777-240_2d5fe924-d0d6-4e50-e063-6294a90a7ab1
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Octisalate, Octocrylene
Dosage form STICK
Route TOPICAL
Labeler BLUEZONWIDE CO.,LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-04-01
Substance OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength 1.05; .67; .3 g/15g; g/15g; g/15g
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 69777-240-02 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 69777-240-02 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69777-240-02 0efc9e666f02…f202fb6c5f17…
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 OrgaPlus Ultra Pure Sun EX
Brand name suffix 15g
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 1.05 g/15g OCTISALATE .67 g/15g OCTOCRYLENE .3 g/15g
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 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69777-240-01 OrgaPlus Ultra Pure Sun EX15g 15 g in 1 CONTAINER STICK 15 2 69777-240-02 OrgaPlus Ultra Pure Sun EX15g 1 in 1 CARTON STICK 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69777-240 ORGAPLUS ULTRA PURE SUN EX 15G (OCTINOXATE, OCTISALATE, OCTOCRYLENE) STICK [BLUEZONWIDE CO.,LTD] 2 Current NDC, Legacy NDC, 2 package rows 20250206_b686ef63-7eee-4a4d-a559-417d8b09cc4f.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 69777-240-01 69777024001 15 g in 1 CONTAINER 15 g Historical 69777-240-02 69777024002 1 CONTAINER in 1 CARTON (69777-240-02) / 15 g in 1 CONTAINER (69777-240-01) 1 container 2018-04-01 0000-00-00 No No Current