FORTE MAGNETIC S3 OIL CONTROL ANTI-DANDFUFF- piroctone olamine lotion/shampoo

FORTE Magnetic S3 Oil Control Anti-Dandfuff by

Drug Labeling and Warnings

FORTE Magnetic S3 Oil Control Anti-Dandfuff by is a Otc medication manufactured, distributed, or labeled by FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Piroctone Olamine 0.4g/500g

PURPOSE

INDICATIONS & USAGE

Uses: Helps prevent recurence of flaking and itching associated with dandruff

WARNINGS

WHEN USING

When using this product:
Avoid contact with eyes.If contact occurs,rinse eyes thoroughly with water.
If accidentally ingested,please seek medical treatment.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

In case of overdose,get medical help or contaet a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:
For best results use at least twice a week or as directed by a doctor.
Wet your hair,and gently massage the scap and roots with an appropriate amount of shampoo,based on your hair quantity.Rinse with
clean water

OTHER SAFETY INFORMATION

Other information:
Store at 5-30C;
Keep out of direct sunlight;
This product contains plant-derived ingredients.Their odor and color may change with temperature and humidity; these changes are nomal;
This product has no magnetic properties, but the ingredients are based on the interaction of opposite charges attracting.

INACTIVE INGREDIENT

Inactive ingredients:

Water (Aqua), Sodium lauroyl Methyl Isethionate, Disodium Laureth Sulfosuccinate, Sodium C14-16 Olefin Sulfonate, Potassium Cocoyl Glycinate, Polysorbate 20, Propylene Glycol, Potassium Cocoate, Cocamidopropyl Betaine, Fragrance, Trisodium Ethylenediamine Disuccinate, Betaine, Ceteareth-60 Myristyl Glycol, Cetrimonium Chloride, Hydroxyacetophenone, Isopropyl Alcohol, Phenoxyethanol, Sodium Lauraminopropionate, Polyquaternium-10, Sodium Chloride, Hexylene Glycol, Caprylhydroxamic Acid, Capryloyl Glycine, Butylene Glycol, Polyquaternium-55, Xylitylglucoside, Glycerin, Sodium Acetate, Enantia Chlorantha Bark Extract, Caprylyl Glycol, Creatine, Glycolic Acid, Polyglyceryl-10 Laurate, Polyquaternium-7, Oleanolic Acid, Sodium Citrate, Sodium Benzoate, Citric Acid, Isostearic Acid

QUESTIONS

Questions?

Dist.By Formosa Biomedical Technology Corporation
formmosabio@fpg.com.tw

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FORTE MAGNETIC S3 OIL CONTROL ANTI-DANDFUFF 
piroctone olamine lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84655-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PIROCTONE OLAMINE (UNII: A4V5C6R9FB) (PIROCTONE - UNII:R49EFA73Q7)	PIROCTONE OLAMINE	0.4 g  in 500 g

Inactive Ingredients
Ingredient Name	Strength
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)
POTASSIUM COCOYL GLYCINATE (UNII: WZ70FUF22U)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
ISOSTEARIC ACID (UNII: X33R8U0062)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CREATINE (UNII: MU72812GK0)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
SODIUM LAUROYL METHYL ISETHIONATE (UNII: II6VCD3S6R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
POLYQUATERNIUM-55 (UNII: NG3KW6CD2J)
OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
SODIUM ACETATE (UNII: 4550K0SC9B)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
BETAINE (UNII: 3SCV180C9W)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCOLIC ACID (UNII: 0WT12SX38S)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FRAGRANCE 13576 (UNII: 5EM498GW35)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
GLYCERIN (UNII: PDC6A3C0OX)
CETEARETH-60 MYRISTYL GLYCOL (UNII: 4O832ZOY6W)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SODIUM LAURAMINOPROPIONATE (UNII: X5NJA9HXPU)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84655-101-02	1 in 1 BOX	08/13/2024
1	NDC: 84655-101-01	500 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/13/2024

Labeler - FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION (658521104)

Establishment
Name	Address	ID/FEI	Business Operations
FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION		658521104	manufacture(84655-101)