warnings
WARNINGS: Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
Borax 200ck
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 200ck
- Generic name
- SODIUM BORATE
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c8d359b2-3ba0-3117-e053-2a95a90aac2f
- SPL ID
- 2dcc6b58-7a86-e2ac-e063-6294a90a9262
- Version
- 4
- Effective date
- 2025-02-10
- Source export date
- 2026-08-01
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
- Import run
- 20260801T225920Z
- Imported at
- 2026-08-01 23:01:14
| Harmonized routes |
|---|
| SUBLINGUAL |
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 200ck | openfda.brand_name | |
| generic name | SODIUM BORATE | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-3006-1 | openfda.package_ndc |
| ndc | product | 76472-3006 | openfda.product_ndc |
| ndc11 | package | 76472300601 | derived:openfda.package_ndc |
| spl id | 2dcc6b58-7a86-e2ac-e063-6294a90a9262 | id | |
| spl set id | c8d359b2-3ba0-3117-e053-2a95a90aac2f | set_id | |
| unii | 91MBZ8H3QO | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.