Borax

Manufacturer: SEVENE USA
Effective date: 2024-01-23
Label type: HUMAN OTC DRUG LABEL
Version: 26
Source: full-release
Hydrated at: 2026-06-01 02:25:50

Label at a glance#

ProductBorax

Active ingredientSODIUM BORATE

Label structure12 sections

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Contacts and useful links#

Websitewww.ollois.com

WWW.OLLOIS.COM

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

HOMEOPATHIC DILUTION OF HPUS Borax 30c.

TRADITIONALLY USED FOR:

OTC - PURPOSE SECTION

Canker sores (mouth ulcers)*

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

USE:

INDICATIONS & USAGE SECTION

Condition listed above or as directed by a physician.

WARNINGS:

WARNINGS SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Store at room temperature.

OTC - DO NOT USE SECTION

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Sucrose.

QUESTIONS?

OTC - QUESTIONS SECTION

INFO@OLLOIS.COM * WWW.OLLOIS.COM * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIC DILUTION MAY NOT BE SUSEPTIBLE TO SCIENTIFIC MEASUREMENT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Img_Borax 30c P2Img_Borax 30c P1

01b lbl Borax 30c P3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76472-1134-1	Borax	80 in 1 CYLINDER	PELLET	80		26

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76472-1134	BORAX (SODIUM BORATE) PELLET [SEVENE USA]	26	Current NDC, Legacy NDC, 1 package rows	20240127_2c24fcda-dcf9-41be-9788-10833d53ab38.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
SODIUM BORATE	ACTIVE INGREDIENT	91MBZ8H3QO	3
BORATE ION	ACTIVE MOIETY	44OAE30D22	3
sucrose	INACTIVE INGREDIENT	C151H8M554	3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Borax
SODIUM BORATE
SUCROSE
BORATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76472-1134	76472-1134-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
SODIUM BORATE	91MBZ8H3QO	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii+route 2 equally ranked IID candidates
sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii+route 2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Borax	SODIUM BORATE	SEVENE USA	2c24fcda-dcf9-41be-9788-10833d53ab38	2024-01-23	Warnings	Exact identifier ndc (package): 76472-1134-1 ndc (product): 76472-1134 ndc11 (package): 76472113401 spl id: 0fa4e7df-771f-3984-e063-6394a90abf72 spl set id: 2c24fcda-dcf9-41be-9788-10833d53ab38

Reported adverse events (FAERS/openFDA)#

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