warnings
Warnings For External Use Only Not for parenteral administration
Saline Ampoules
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
- Saline Ampoules
- Generic name
- SODIUM CHLORIDE 0.9%
- Manufacturer
- Trifecta Pharmaceuticals USA, LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ee18ef7c-bb5d-30ec-e053-2a95a90a964e
- SPL ID
- 410d90c1-c459-8577-e063-6394a90a8254
- Version
- 3
- Effective date
- 2025-10-13
- Source export date
- 2026-10-30
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:34:37
| 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 |
|---|---|---|---|
| brand name | Saline Ampoules | openfda.brand_name | |
| generic name | SODIUM CHLORIDE 0.9% | openfda.generic_name | |
| manufacturer name | Trifecta Pharmaceuticals USA, LLC. | openfda.manufacturer_name | |
| ndc | package | 69396-116-05 | openfda.package_ndc |
| ndc | product | 69396-116 | openfda.product_ndc |
| ndc11 | package | 69396011605 | derived:openfda.package_ndc |
| rxcui | 351179 | openfda.rxcui | |
| spl id | 410d90c1-c459-8577-e063-6394a90a8254 | id | |
| spl set id | ee18ef7c-bb5d-30ec-e053-2a95a90a964e | 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.