NATRUM SULPHURICUM- disodium sulfate granule

NATRUM SULPHURICUM by

Drug Labeling and Warnings

NATRUM SULPHURICUM 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

NATRUM SULPHURICUM (Disodium sulfate) 12CH GR

NATRUM SULPHURICUM (Disodium sulfate) 15CH GR

NATRUM SULPHURICUM (Disodium sulfate) 200K GR

NATRUM SULPHURICUM (Disodium sulfate) 30CH GR

NATRUM SULPHURICUM (Disodium sulfate) 30K GR

NATRUM SULPHURICUM (Disodium sulfate) MK GR

NATRUM SULPHURICUM (Disodium sulfate) XMK GR

PURPOSE

Indications

For the temporary relief of food craving and
headache

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 food craving and
headache

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 : 62106-5220-4

NATRUM SULPHURICUM

Disodium sulfate

140 granules

Indications

For the temporary relief of food craving and
headache

INGREDIENTS AND APPEARANCE

NATRUM SULPHURICUM 
disodium sulfate granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-5220
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)	SODIUM SULFATE	1 [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: 62106-5220-4	10 in 1 CARTON	01/29/2015
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		01/29/2015

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-5220)