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 (canonical bytes are SHA-256 checked before publication)

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: 2026-09-28
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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:27

Harmonized routes table
Harmonized routes
SUBLINGUAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
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

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

WARNINGS: Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Adverse event summaries are temporarily unavailable. Other product information remains available.