warnings
Warnings · NOT FOR INJECTION · Do not use if the ampoule is damaged or already open · Do not use after expiration date · Discontinue if you experience any adverse reaction and call your physician · Keep out of reach of children
WHWSWB 0.9% Saline
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
- WHWSWB 0.9% Saline
- Generic name
- SODIUM CHLORIDE
- Manufacturer
- Yiwu Huanshu E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4e9c21e5-f2f9-90e4-e063-6394a90acfe2
- SPL ID
- 565825ff-6d64-606b-e063-6294a90a56aa
- Version
- 2
- Effective date
- 2026-07-11
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:37
| Harmonized routes |
|---|
| NASAL |
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 | WHWSWB 0.9% Saline | openfda.brand_name | |
| generic name | SODIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Yiwu Huanshu E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 87561-001-00 | openfda.package_ndc |
| ndc | product | 87561-001 | openfda.product_ndc |
| ndc11 | package | 87561000100 | derived:openfda.package_ndc |
| spl id | 565825ff-6d64-606b-e063-6294a90a56aa | id | |
| spl set id | 4e9c21e5-f2f9-90e4-e063-6394a90acfe2 | set_id | |
| unii | LYR4M0NH37 | 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.