Borax
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
- Borax
- Generic name
- SODIUM BORATE
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 848920e1-6b74-5db4-e053-2991aa0ab118
- SPL ID
- f2f61a3b-d202-b356-e053-2995a90aa9d0
- Version
- 2
- Effective date
- 2023-01-23
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:28:15
| Harmonized routes |
|---|
| ORAL |
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 | Borax | openfda.brand_name | |
| generic name | SODIUM BORATE | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-0881-41 | openfda.package_ndc |
| ndc | product | 0220-0881 | openfda.product_ndc |
| ndc11 | package | 00220088141 | derived:openfda.package_ndc |
| spl id | f2f61a3b-d202-b356-e053-2995a90aa9d0 | id | |
| spl set id | 848920e1-6b74-5db4-e053-2991aa0ab118 | set_id | |
| unii | 91MBZ8H3QO | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.