STOMASIN- gypsum fibrosum extract, forsythia viridissima fruit extract, arctium lappa fruit extract, platycodon grandiflorus root extract, saposhnikovia divaricata root extract, glycyrrhiza uralensis root extract, ostericum koreanum extract, schizonepeta tenuifolia extract capsule, coated

Stomasin by

Drug Labeling and Warnings

Stomasin by is a Homeopathic medication manufactured, distributed, or labeled by MedicareBio.Co.Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Gypsum fibrosum extract, Forsythia viridissima fruit extract, Arctium lappa fruit extract, Platycodon grandiflorus root extract, Saposhnikovia divaricata root extract, Glycyrrhiza uralensis root extract, Ostericum koreanum extract, Schizonepeta tenuifolia extract

Purpose

antipyretic, anti-inflammatory, anti-corona virus (omicron variant)

Uses

for swelling and sore throat symptoms

temporarily reduces fever; relieves swelling and sore throat for tonsillitis / peritonsillitis

Warnings

Do not use in the following patients
Because this drug contains lactose, it should not be administered to patients with genetic problems such as galactose intolerance, lactose intolerance, or glucose-galactose malabsorption.: See Insert Paper

Warnings

Keep out of reach of children

Warnings

In the following cases, stop using this drug immediately and consult a doctor, carry this Insert Paper with you. : See Insert Paper

Warnings

The following people should not use this drug. Infants under 3 months

The following people should consult with a doctor before use if you have .: See Insert Paper

Warnings

Storage precautions : See Insert Paper

If pregnant or breast-feeding, ask a health professional before use

In case of overdose, get medical help or contact a Poison Control Center immediately

Directions

Adults Take 2 capsules per time, 3 times a day
Children 7 years to under 14 years 2/3 of the adult dose (4/3 capsules)
Children 4 years to under 6 years 1/2 of the adult dose (1 capsule)
Children 2 years to under 3 years 1/3 of the adult dose (2/3 capsule)
Children under 1 years 1/4 of the adult dose (1/2 capsule)
Dissolve it in lukewarm water before or between meals (between meals and between meals) and take it slowly in small portions while moistening the mouth or throat (do not swallow capsules).

Other Information

protect from excessive moisture, store at 1~30℃(33.8~86℉)

Inactive Ingredients

FD&C blue no.1, FD&C blue no.3, FD&C yellow no.5, lactose hydrate (cow, milk), magnesium stearate, silicon dioxide, gelatin

Display Panel

INGREDIENTS AND APPEARANCE

STOMASIN 
gypsum fibrosum extract, forsythia viridissima fruit extract, arctium lappa fruit extract, platycodon grandiflorus root extract, saposhnikovia divaricata root extract, glycyrrhiza uralensis root extract, ostericum koreanum extract, schizonepeta tenuifolia extract capsule, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82871-301
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OSTERICUM GROSSESERRATUM ROOT (UNII: 9IGM98814N) (OSTERICUM GROSSESERRATUM ROOT - UNII:9IGM98814N)	OSTERICUM GROSSESERRATUM ROOT	250 mg
CALCIUM SULFATE, UNSPECIFIED FORM (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE, UNSPECIFIED FORM	1665 mg
FORSYTHIA VIRIDISSIMA FRUIT (UNII: P4ZY00SWES) (FORSYTHIA VIRIDISSIMA FRUIT - UNII:P4ZY00SWES)	FORSYTHIA VIRIDISSIMA FRUIT	835 mg
ARCTIUM LAPPA FRUIT (UNII: EA541308MV) (ARCTIUM LAPPA FRUIT - UNII:EA541308MV)	ARCTIUM LAPPA FRUIT	500 mg
PLATYCODON GRANDIFLORUM ROOT (UNII: 2DF0NS0O2Z) (PLATYCODON GRANDIFLORUM ROOT - UNII:2DF0NS0O2Z)	PLATYCODON GRANDIFLORUM ROOT	500 mg
SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD) (SAPOSHNIKOVIA DIVARICATA ROOT - UNII:8H84LFK2QD)	SAPOSHNIKOVIA DIVARICATA ROOT	500 mg
NEPETA TENUIFOLIA FLOWERING TOP (UNII: 2FN3BA1MZE) (NEPETA TENUIFOLIA FLOWERING TOP - UNII:2FN3BA1MZE)	NEPETA TENUIFOLIA FLOWERING TOP	250 mg
GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K) (GLYCYRRHIZA URALENSIS ROOT - UNII:42B5YD8F0K)	GLYCYRRHIZA URALENSIS ROOT	250 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
MAGNESIUM STEARATE (UNII: 70097M6I30)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)

Product Characteristics
Color	blue (blue and dark green capsule)	Score	score with uneven pieces
Shape	CAPSULE (brown powder encapsulated in blue and dark green opaque capsule)	Size	22mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82871-301-01	10 in 1 BLISTER PACK; Type 0: Not a Combination Product	07/13/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/13/2022

Labeler - MedicareBio.Co.Ltd (695630697)

Registrant - MedicareBio.Co.Ltd (695630697)

Establishment
Name	Address	ID/FEI	Business Operations
MedicareBio.Co.Ltd		695630697	manufacture(82871-301)