SULPHUR- sublimed sulfur granule

SULPHUR by

Drug Labeling and Warnings

SULPHUR 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

SULPHUR (Sublimed sulfur) 12CH GR

SULPHUR (Sublimed sulfur) 15CH GR

SULPHUR (Sublimed sulfur) 200CH GR

SULPHUR (Sublimed sulfur) 200K GR

SULPHUR (Sublimed sulfur) 30CH GR

SULPHUR (Sublimed sulfur) 30K GR

SULPHUR (Sublimed sulfur) 5CH GR

SULPHUR (Sublimed sulfur) 7CH GR

SULPHUR (Sublimed sulfur) 9CH GR

SULPHUR (Sublimed sulfur) MK GR

SULPHUR (Sublimed sulfur) XMK GR

PURPOSE

Indications

For the temporary relief of skin irritations

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 skin irritations

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 : 62106-5316-4

SULPHUR

Sublimed sulfur

140 granules

Indications

For the temporary relief of skin irritations

INGREDIENTS AND APPEARANCE

SULPHUR 
sublimed sulfur granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-5316
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	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: 62106-5316-4	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(62106-5316)