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 (canonical bytes are SHA-256 checked before publication)

Brand name: BORAX
Generic name: BORAX
Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product type: HUMAN OTC DRUG
SPL set ID: a3d8768d-6fd9-4a7d-9143-5397308fa331
SPL ID: cd134645-8fef-c941-e053-2a95a90af7fe
Version: 3
Effective date: 2021-09-28
Source export date: 2026-10-27
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:10:53

Harmonized routes table
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.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		BORAX	openfda.brand_name
generic name		BORAX	openfda.generic_name
manufacturer name		Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	openfda.manufacturer_name
ndc	package	15631-0084-2	openfda.package_ndc
ndc	package	15631-0084-5	openfda.package_ndc
ndc	package	15631-0084-6	openfda.package_ndc
ndc	package	15631-0084-3	openfda.package_ndc
ndc	package	15631-0084-1	openfda.package_ndc
ndc	package	15631-0084-7	openfda.package_ndc
ndc	package	15631-0084-0	openfda.package_ndc
ndc	package	15631-0084-4	openfda.package_ndc
ndc	product	15631-0084	openfda.product_ndc
ndc11	package	15631008400	derived:openfda.package_ndc
ndc11	package	15631008403	derived:openfda.package_ndc
ndc11	package	15631008407	derived:openfda.package_ndc
ndc11	package	15631008401	derived:openfda.package_ndc
ndc11	package	15631008406	derived:openfda.package_ndc
ndc11	package	15631008404	derived:openfda.package_ndc
ndc11	package	15631008402	derived:openfda.package_ndc
ndc11	package	15631008405	derived:openfda.package_ndc
spl id		cd134645-8fef-c941-e053-2a95a90af7fe	id
spl set id		a3d8768d-6fd9-4a7d-9143-5397308fa331	set_id
unii		91MBZ8H3QO	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children Do not use if capseal is broken or missing. Close the cap tightly after use.

Reported adverse events (FAERS/openFDA)#

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