warnings
For external use only Do not use on damaged or broken skin When using this product, keep out of eyes. Rinse with water to remove. Stop using and ask a doctor if rash occurs.
JUNGSAEMMOOL Essential Skin Nuder Cushion N-Light
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
- Brand name
- JUNGSAEMMOOL Essential Skin Nuder Cushion N-Light
- Generic name
- TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
- Manufacturer
- Jungsaemmool Beauty Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cf7c4445-0382-47ab-aba9-b40d63e4f1cc
- SPL ID
- 4fa83367-cc53-9e2a-e063-6294a90ad3fa
- Version
- 2
- Effective date
- 2026-04-17
- Source export date
- 2026-10-27
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:07:26
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | JUNGSAEMMOOL Essential Skin Nuder Cushion N-Light | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE | openfda.generic_name | |
| manufacturer name | Jungsaemmool Beauty Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 71261-032-01 | openfda.package_ndc |
| ndc | package | 71261-032-03 | openfda.package_ndc |
| ndc | package | 71261-032-02 | openfda.package_ndc |
| ndc | package | 71261-032-05 | openfda.package_ndc |
| ndc | package | 71261-032-04 | openfda.package_ndc |
| ndc | product | 71261-032 | openfda.product_ndc |
| ndc11 | package | 71261003202 | derived:openfda.package_ndc |
| ndc11 | package | 71261003203 | derived:openfda.package_ndc |
| ndc11 | package | 71261003201 | derived:openfda.package_ndc |
| ndc11 | package | 71261003204 | derived:openfda.package_ndc |
| ndc11 | package | 71261003205 | derived:openfda.package_ndc |
| spl id | 4fa83367-cc53-9e2a-e063-6294a90ad3fa | id | |
| spl set id | cf7c4445-0382-47ab-aba9-b40d63e4f1cc | set_id | |
| unii | 15FIX9V2JP | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii | |
| unii | 4Y5P7MUD51 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.