SULPHUR- sublimed sulfur granule 
Seroyal USA

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

SULPHUR

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

Indications

For the temporary relief of skin irritations

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.

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.

Inactive Ingredients

Lactose,

sucrose.

Directions

Adults: Take five granules three times daily or as recommended by your healthcare practitioner.

Children: Take three granules and follow adult directions.

QUESTIONS? 1-888-737-6925.

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.

62106-5316

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

SULPHUR 
sublimed sulfur granule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-5316
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR1 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62106-5316-410 in 1 CARTON01/30/2015
1140 in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/30/2015
Labeler - Seroyal USA (018361118)
Establishment
NameAddressID/FEIBusiness Operations
SAN’UP401010287manufacture(62106-5316)

Revised: 11/2022
 
Seroyal USA