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NOT FOR DIRECT INJECTION
Sterile Water
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
- Sterile Water
- Generic name
- WATER
- Manufacturer
- American Regent, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 78b35864-4bbc-4759-a5c1-7e4f25e22932
- SPL ID
- b885fb92-786e-49bf-aed2-17b430e4743e
- Version
- 8
- Effective date
- 2022-01-31
- 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 05:52:10
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | Sterile Water | openfda.brand_name | |
| generic name | WATER | openfda.generic_name | |
| manufacturer name | American Regent, Inc. | openfda.manufacturer_name | |
| ndc | package | 0517-3020-25 | openfda.package_ndc |
| ndc | package | 0517-3005-25 | openfda.package_ndc |
| ndc | package | 0517-3010-25 | openfda.package_ndc |
| ndc | package | 0517-3005-01 | openfda.package_ndc |
| ndc | package | 0517-3020-01 | openfda.package_ndc |
| ndc | package | 0517-3010-01 | openfda.package_ndc |
| ndc | product | 0517-3010 | openfda.product_ndc |
| ndc | product | 0517-3020 | openfda.product_ndc |
| ndc | product | 0517-3005 | openfda.product_ndc |
| ndc11 | package | 00517300525 | derived:openfda.package_ndc |
| ndc11 | package | 00517301001 | derived:openfda.package_ndc |
| ndc11 | package | 00517302001 | derived:openfda.package_ndc |
| ndc11 | package | 00517300501 | derived:openfda.package_ndc |
| ndc11 | package | 00517302025 | derived:openfda.package_ndc |
| ndc11 | package | 00517301025 | derived:openfda.package_ndc |
| spl id | b885fb92-786e-49bf-aed2-17b430e4743e | id | |
| spl set id | 78b35864-4bbc-4759-a5c1-7e4f25e22932 | set_id | |
| unii | 059QF0KO0R | openfda.unii |
Boxed warning 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.