BORAX- sodium borate pellet

Borax by

Drug Labeling and Warnings

Borax by is a Homeopathic medication manufactured, distributed, or labeled by HBC NATURALS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

HOMEOPATHIC DILUTION OF HPUS Borax 30c.

TRADITIONALLY USED FOR:

CANKER SORES (MOUTH ULCERS)

DIRECTIONS:

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

USE:

Condition listed above or as directed by a physician.

WARNINGS:

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

PREGNANCY OR BREAST FEEDING

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OTHER INFORMATION:

Store at room temperature.

DO NOT USE

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENTS:

Sucrose.

QUESTIONS?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BORAX 
sodium borate pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76472-1134
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	30 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
sucrose (UNII: C151H8M554)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76472-1134-1	80 in 1 CYLINDER; Type 0: Not a Combination Product	11/30/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/30/2011

Labeler - HBC NATURALS INC (969332936)