warnings
Warnings For external use only - Do not use if solution changes color or becomes cloudy - Do not touch the tip of the container to any surface to avoid contamination
OHTrust Artifical Eyedrop
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
- OHTrust Artifical Eyedrop
- Generic name
- SODIUM CHLORIDE
- Manufacturer
- Nanoplus Technology Co., Limited
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2ea26d96-704b-17bb-e063-6394a90a7e27
- SPL ID
- 558c1535-5f99-4f6e-e063-6294a90aa382
- Version
- 2
- Effective date
- 2026-07-01
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:45
| Harmonized routes |
|---|
| OPHTHALMIC |
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 | M018 | openfda.application_number | |
| brand name | OHTrust Artifical Eyedrop | openfda.brand_name | |
| generic name | SODIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Nanoplus Technology Co., Limited | openfda.manufacturer_name | |
| ndc | package | 70970-008-01 | openfda.package_ndc |
| ndc | product | 70970-008 | openfda.product_ndc |
| ndc11 | package | 70970000801 | derived:openfda.package_ndc |
| rxcui | 2706648 | openfda.rxcui | |
| spl id | 558c1535-5f99-4f6e-e063-6294a90aa382 | id | |
| spl set id | 2ea26d96-704b-17bb-e063-6394a90a7e27 | set_id | |
| unii | 451W47IQ8X | 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.