SILICEA by Seroyal USA / SAN’UP SILICEA- silica granule

SILICEA by

Drug Labeling and Warnings

SILICEA 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 Ingredient

SILICEA (Silica) 12CH GR

SILICEA (Silica) 15CH GR

SILICEA (Silica) 200CH GR

SILICEA (Silica) 200K GR

SILICEA (Silica) 30CH GR

SILICEA (Silica) 30K GR

SILICEA (Silica) 5CH GR

SILICEA (Silica) 7CH GR

SILICEA (Silica) 9CH GR

SILICEA (Silica) CMK GR

SILICEA (Silica) MK GR

SILICEA (Silica) XMK GR

PURPOSE

Indications

For the temporary relief of general fatigue
symptoms

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 general fatigue
symptoms

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 : 62106-5301-4

SILICEA

Silica

140 granules

Indications

For the temporary relief of general fatigue
symptoms

INGREDIENTS AND APPEARANCE

SILICEA 
silica granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-5301
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	2 [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: 62106-5301-4	10 in 1 CARTON	01/30/2015
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		01/30/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-5301)