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 Pink 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 Pink Light
- Generic name
- TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
- Manufacturer
- Jungsaemmool Beauty Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4a09a01a-404f-4b67-91e0-666153f550e8
- SPL ID
- 4fa83367-cc52-9e2a-e063-6294a90ad3fa
- Version
- 2
- Effective date
- 2026-04-17
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:22
| 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 Pink Light | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE | openfda.generic_name | |
| manufacturer name | Jungsaemmool Beauty Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 71261-031-02 | openfda.package_ndc |
| ndc | package | 71261-031-01 | openfda.package_ndc |
| ndc | package | 71261-031-03 | openfda.package_ndc |
| ndc | package | 71261-031-04 | openfda.package_ndc |
| ndc | package | 71261-031-05 | openfda.package_ndc |
| ndc | product | 71261-031 | openfda.product_ndc |
| ndc11 | package | 71261003103 | derived:openfda.package_ndc |
| ndc11 | package | 71261003104 | derived:openfda.package_ndc |
| ndc11 | package | 71261003101 | derived:openfda.package_ndc |
| ndc11 | package | 71261003105 | derived:openfda.package_ndc |
| ndc11 | package | 71261003102 | derived:openfda.package_ndc |
| spl id | 4fa83367-cc52-9e2a-e063-6294a90ad3fa | id | |
| spl set id | 4a09a01a-404f-4b67-91e0-666153f550e8 | 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.