THIOSINAMINUM- thiosinamine granule

THIOSINAMINUM by

Drug Labeling and Warnings

THIOSINAMINUM 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

THIOSINAMINUM 30CH GR

THIOSINAMINUM 30K GR

THIOSINAMINUM 5CH GR

PURPOSE

Indications

For the temporary relief of dizziness

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.

INDICATIONS & USAGE

Indications

For the temporary relief of dizziness

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.

PRINCIPAL DISPLAY PANEL

UNDA
Do not use if label perforation is broken
Homeopathic Remedy
NDC : 62106-6482-4
THIOSINAMINUM
Thiosinamine
140 granules
Indications

For the temporary relief of dizziness

INGREDIENTS AND APPEARANCE

THIOSINAMINUM 
thiosinamine granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-6482
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7)	ALLYLTHIOUREA	3 [hp_X]

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62106-6482-4	10 in 1 CARTON	07/15/2015
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		07/15/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-6482)