OrgaPlus Ultra Pure Sun EX 22g

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
OrgaPlus Ultra Pure Sun EX 22g
Generic name
OCTINOXATE, OCTISALATE, OCTOCRYLENE
Manufacturer
BLUEZONWIDE CO.,LTD
Product type
HUMAN OTC DRUG
SPL set ID
d3c422f6-a83d-48fc-94fc-2749666426c8
SPL ID
2d602c5f-384c-b003-e063-6294a90afd2e
Version
2
Effective date
2025-02-05
Source export date
2026-10-27
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 21:07:08
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Warnings: -For external use only -Protect the product in the container from excessive heat and direct sun. -When using this product keep out of eyes. -Stop use and ask a doctor if rash occurs.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.