IGATAN F- coated ascorbic acid, tocopherol acetate, carbazochrome, lysozyme chloride capsule

IGATAN F by

Drug Labeling and Warnings

IGATAN F by is a Otc medication manufactured, distributed, or labeled by OASIS TRADING. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

COATED ASCORBIC ACID, TOCOPHEROL ACETATE, CARBAZOCHROME, LYSOZYME CHLORIDE

PURPOSE

Preventing further damage to the gum tissue

Anti-inflammatory and Hemostatic action

Synergistic effect of periodontal disease treatment

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Adults: Take one capsule three times a day after meals.

WARNINGS

Please refer to the leaflet enclosed.

INACTIVE INGREDIENT

Corn starch, Lactose hydrate, Microcrystalline cellulose, Sodium starch glycolate, Colloidal silicon dioxide, Magnesium stearate, Capsule, Sunset yellow FCF, Quinoline yellow WS

DOSAGE & ADMINISTRATION

For oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IGATAN F 
coated ascorbic acid, tocopherol acetate, carbazochrome, lysozyme chloride capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72689-0027
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	156 mg
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL ACETATE	10 mg
CARBAZOCHROME (UNII: 81F061RQS4) (CARBAZOCHROME - UNII:81F061RQS4)	CARBAZOCHROME	2 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	yellow	Score	no score
Shape	CAPSULE	Size	18mm
Flavor		Imprint Code	IgatanF
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72689-0027-1	100 in 1 BLISTER PACK; Type 0: Not a Combination Product	11/23/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/20/2018

Labeler - OASIS TRADING (689991468)

Registrant - OASIS TRADING (689991468)

Establishment
Name	Address	ID/FEI	Business Operations
OASIS TRADING		689991468	manufacture(72689-0027) , relabel(72689-0027)