BORAX- sodium borate granule

BORAX by

Drug Labeling and Warnings

BORAX by is a Homeopathic medication manufactured, distributed, or labeled by Seroyal USA, SAN’UP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

BORAX 200K GR

BORAX 30CH GR

BORAX 30K GR

BORAX 5CH GR

PURPOSE

Indications

For the temporary relief of motion sickness, nausea,
and diarrhea

WARNINGS

Warning:
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OVERDOSAGE

In case of overdose, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive Ingredients
Lactose,
sucrose.

DOSAGE & ADMINISTRATION

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

QUESTIONS

QUESTIONS? 1-888-737-6925.

INDICATIONS & USAGE

Indications

For the temporary relief of motion sickness, nausea,
and diarrhea

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

PRINCIPAL DISPLAY PANEL

UNDA
Do not use if label perforation is broken
Homeopathic Remedy
NDC : 62106-4925-4
BORAX
Sodium borate
140 granules
Indications

For the temporary relief of motion sickness, nausea,
and diarrhea

INGREDIENTS AND APPEARANCE

BORAX 
sodium borate granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-4925
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	1 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62106-4925-4	10 in 1 CARTON	06/11/2015
1		140 in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/11/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-4925)