81736-0001_Dr.FORHAIR FOLLIGEN SHAMPOO

Dr.FORHAIR FOLLIGEN by

Drug Labeling and Warnings

Dr.FORHAIR FOLLIGEN by is a Otc medication manufactured, distributed, or labeled by Wyatt Co., Ltd., Cosmocos Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR.FORHAIR FOLLIGEN- pyrithione zinc, salicylic acid shampoo 
Wyatt Co., Ltd.

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81736-0001_Dr.FORHAIR FOLLIGEN SHAMPOO

zinc pyrithione 0.288%

Salicylic Acid 0.2%

Water, Disodium Laureth Sulfosuccinate, Lauryl Hydroxysultaine, Cocamide Methyl MEA, Styrene/Acrylates Copolymer, Glycerin, Sodium Cocoyl Isethionate, PEG-120 Methyl Glucose Dioleate, Propanediol, Fragrance, Sodium Lauroyl Methylaminopropionate, Alcohol, PEG-45 Palm Kernel Glycerides, Panthenol, C12-13 Alkyl Lactate, Polyquaternium-10, Cetrimonium Chloride, Menthol, Cocamidopropyl Betaine, Caprylyl Glycol, Trihydroxystearin, Disodium EDTA, Zinc Chloride, Sodium Benzoate, Polyquaternium-7, PEG-6 Caprylic/Capric Glycerides, Ethylhexylglycerin, Sodium Chloride, Citric Acid, Camellia Japonica Seed Oil, Argania Spinosa Kernel Oil, Adenosine, Disodium Phosphate, Niacinamide, Moringa Oleifera Seed Oil, Tocopherol, Biotin, Ceramide NP, Lecithin, Caprylic/Capric Triglyceride, Polysorbate 80, Serenoa Serrulata Fruit Extract, Caffeic Acid, Rhodiola Rosea Root Extract, Dioscorea Japonica Root Extract, Paeonia Lactiflora Root Extract, Zingiber Officinale (Ginger) Root Extract, Sophora Flavescens Extract, 1,2-Hexanediol

Anti-dandruff

keep out or reach of the children

Helps prevent recurrence of flaking and itching associated with dandruff

For external use only.

When using this product, do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

Apply to wet hair. Work into a rich lather and gently massage into scalp and hair. Rinse thoroughly with lukewarm water.

DR.FORHAIR FOLLIGEN 
pyrithione zinc, salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81736-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	2.88 g  in 100 mL
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
LAURYL HYDROXYSULTAINE (UNII: 176KKP31OZ)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM LAUROYL METHYLAMINOPROPIONATE (UNII: 99E3R68Y9B)
ALCOHOL (UNII: 3K9958V90M)
PEG-45 PALM KERNEL GLYCERIDES (UNII: UC117W498W)
PANTHENOL (UNII: WV9CM0O67Z)
C12-13 ALKYL LACTATE (UNII: 9GLX7JL13M)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ZINC CHLORIDE (UNII: 86Q357L16B)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
ARGAN OIL (UNII: 4V59G5UW9X)
ADENOSINE (UNII: K72T3FS567)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
NIACINAMIDE (UNII: 25X51I8RD4)
MORINGA OLEIFERA SEED OIL (UNII: REM6A5QMC0)
TOCOPHEROL (UNII: R0ZB2556P8)
BIOTIN (UNII: 6SO6U10H04)
CERAMIDE NP (UNII: 4370DF050B)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SAW PALMETTO (UNII: J7WWH9M8QS)
CAFFEIC ACID (UNII: U2S3A33KVM)
SEDUM ROSEUM ROOT (UNII: 3S5ITS5ULN)
DIOSCOREA JAPONICA TUBER (UNII: I43FCF3356)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
GINGER (UNII: C5529G5JPQ)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81736-0001-2	1 in 1 CARTON	03/27/2021	01/31/2024
1	NDC: 81736-0001-1	750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 81736-0001-5	2 in 1 CARTON	08/16/2023	01/31/2024
2	NDC: 81736-0001-1	750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 81736-0001-4	1 in 1 CARTON	04/14/2022	01/31/2024
3	NDC: 81736-0001-3	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	03/27/2021	01/31/2024

Labeler - Wyatt Co., Ltd. (688361281)

Registrant - Wyatt Co., Ltd. (688361281)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmocos Co., Ltd		689387376	manufacture(81736-0001)

Revised: 1/2024

Document Id: 0e78023c-a3f5-77c4-e063-6294a90a246f

34390-5

Set id: b1ca4b69-bf03-4cae-89b7-47af15917a3d

Version: 7

Effective Time: 20240108