Therapytion Nokmosu Neutral and oily Hair

Manufacturer: Therapytion Co., Ltd.
Effective date: 2014-04-29
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:39:10

Label at a glance#

ProductTherapytion Nokmosu Neutral and oily Hair

Active ingredientPYRITHIONE ZINC, PANTHENOL, NIACINAMIDE, BIOTIN

Label structure1 sections

Label contents#

Full prescribing information#

Therapytion Nokmosu Neutral and oily Hair shampoo

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

zinc pyrithione, panthenol, niacinamide, biotin

OTC - ACTIVE INGREDIENT SECTION

To recover the scalp condition for healthier hair. To strengthen hair root, give growth stimulation and thicken hair

OTC - PURPOSE SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63214-102-02	2019-11-27	C162847	48780-1	9855e2a2-4185-60a7-e053-dbdaa90a05bd	Therapytion Nokmosu Neutral and oily Hair shampoo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63214-102-01	Therapytion Nokmosu Neutral and oily Hair	530 g in 1 BOTTLE, PLASTIC	SHAMPOO	530		3
63214-102-02	Therapytion Nokmosu Neutral and oily Hair	1 in 1 CARTON	SHAMPOO	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63214-102	THERAPYTION NOKMOSU NEUTRAL AND OILY HAIR (ZINC PYRITHIONE, PANTHENOL, NIACINAMIDE, BIOTIN) SHAMPOO [THERAPYTION CO., LTD.]	3	Legacy NDC, 2 package rows	20140501_a946566d-70f3-42a5-8e27-c1f67c5f40d5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BIOTIN	ACTIVE INGREDIENT	6SO6U10H04	3
NIACINAMIDE	ACTIVE INGREDIENT	25X51I8RD4	3
PANTHENOL	ACTIVE INGREDIENT	WV9CM0O67Z	3
PYRITHIONE ZINC	ACTIVE INGREDIENT	R953O2RHZ5	3
BIOTIN	ACTIVE MOIETY	6SO6U10H04	3
NIACINAMIDE	ACTIVE MOIETY	25X51I8RD4	3
PANTHENOL	ACTIVE MOIETY	WV9CM0O67Z	3
PYRITHIONE ZINC	ACTIVE MOIETY	R953O2RHZ5	3
Ammonium lauryl sulfate	INACTIVE INGREDIENT	Q7AO2R1M0B	3
Benzophenone-9	INACTIVE INGREDIENT	7925W14T4L	3
Caramel	INACTIVE INGREDIENT	T9D99G2B1R	3
CITRIC ACID ACETATE	INACTIVE INGREDIENT	DSO12WL7AU	3
Cocamidopropyl Betaine	INACTIVE INGREDIENT	5OCF3O11KX	3
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	3
DISODIUM EDTA-COPPER	INACTIVE INGREDIENT	6V475AX06U	3
GLYCYRRHIZA GLABRA WHOLE	INACTIVE INGREDIENT	M1F96IE0ZC	3
PANAX GINSENG ROOT OIL	INACTIVE INGREDIENT	P9T4K47OM0	3
PEG-6 COCAMIDE	INACTIVE INGREDIENT	YZ6NLA4O1E	3
PEG-7 Glyceryl Cocoate	INACTIVE INGREDIENT	VNX7251543	3
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	3
Sodium Laureth Sulfate	INACTIVE INGREDIENT	BPV390UAP0	3
SOYBEAN	INACTIVE INGREDIENT	L7HT8F1ZOD	3
SWERTIA JAPONICA	INACTIVE INGREDIENT	01X0P6GX6C	3
Water	INACTIVE INGREDIENT	059QF0KO0R	3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

Therapytion Nokmosu Neutral and oily Hair
zinc pyrithione, panthenol, niacinamide, biotin
PYRITHIONE ZINC
PANTHENOL
NIACINAMIDE
BIOTIN
Water
Sodium Laureth Sulfate
Ammonium lauryl sulfate
Cocamidopropyl Betaine
PEG-6 COCAMIDE
SOYBEAN
PEG-7 Glyceryl Cocoate
DIMETHICONE
Sodium Chloride
SWERTIA JAPONICA
GLYCYRRHIZA GLABRA WHOLE
PANAX GINSENG ROOT OIL
CITRIC ACID ACETATE
DISODIUM EDTA-COPPER
Benzophenone-9
Caramel

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63214-102	63214-102-01, 63214-102-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PYRITHIONE ZINC	R953O2RHZ5	ACTIB
PANTHENOL	WV9CM0O67Z	ACTIB
NIACINAMIDE	25X51I8RD4	ACTIB
BIOTIN	6SO6U10H04	ACTIB
Water	059QF0KO0R	IACT
Sodium Laureth Sulfate	BPV390UAP0	IACT
Ammonium lauryl sulfate	Q7AO2R1M0B	IACT
Cocamidopropyl Betaine	5OCF3O11KX	IACT
PEG-6 COCAMIDE	YZ6NLA4O1E	IACT
SOYBEAN	L7HT8F1ZOD	IACT
PEG-7 Glyceryl Cocoate	VNX7251543	IACT
DIMETHICONE	92RU3N3Y1O	IACT
Sodium Chloride	451W47IQ8X	IACT
SWERTIA JAPONICA	01X0P6GX6C	IACT
GLYCYRRHIZA GLABRA WHOLE	M1F96IE0ZC	IACT
PANAX GINSENG ROOT OIL	P9T4K47OM0	IACT
CITRIC ACID ACETATE	DSO12WL7AU	IACT
DISODIUM EDTA-COPPER	6V475AX06U	IACT
Benzophenone-9	7925W14T4L	IACT
Caramel	T9D99G2B1R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 3 · 153 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION/ DROPS / AURICULAR (OTIC)		3 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / EPIDURAL		648 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRASYNOVIAL	0.9 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / INTRATYMPANIC		2 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	LIQUID / SUBCUTANEOUS	0.7 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, FOR SOLUTION / INTRATHECAL	1.35 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOAP / TOPICAL	1.26 %w/w		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION / INTRALESIONAL		13 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION / INTRA-ARTICULAR		26 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / INTRAVASCULAR	NA		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / SUBMUCOSAL	16 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Ammonium lauryl sulfate	AMMONIUM LAURYL SULFATE	Q7AO2R1M0B	AEROSOL / TOPICAL	NA		Exact identifier — unii candidate 3 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / DENTAL	0.4 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / SUBCUTANEOUS	0.8 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / RESPIRATORY (INHALATION)		108 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SYRUP / ORAL		40 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Caramel	CARAMEL	T9D99G2B1R	SOLUTION / ORAL		11 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
SOYBEAN	SOYBEAN	L7HT8F1ZOD	CAPSULE / ORAL	NA		Exact identifier — unii candidate 2 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	CAPSULE / ORAL		6 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, FOR SUSPENSION / INTRA-ARTICULAR		45 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUPPOSITORY / RECTAL		140 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Caramel	CARAMEL	T9D99G2B1R	GRANULE, FOR SUSPENSION / ORAL	2.5 mg/5ml		Exact identifier — unii candidate 9 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	LIQUID / INTRAVENOUS		6320 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / RESPIRATORY (INHALATION)		43 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	POWDER, FOR SOLUTION / OPHTHALMIC	0.9 %w/w		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / TOPICAL		210 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Caramel	CARAMEL	T9D99G2B1R	SUSPENSION / ORAL	111.12 mg/5ml		Exact identifier — unii candidate 9 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	DROPS / NASAL	NA		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / OPHTHALMIC		13 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRACAVITARY	0.82 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SPRAY, METERED / NASAL		36 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	TABLET, ORALLY DISINTEGRATING / ORAL		10 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	GEL / VAGINAL	10 %w/w		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / ORAL		148 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		1800 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Laureth Sulfate	SODIUM LAURETH-3 SULFATE	BPV390UAP0	SPRAY / TOPICAL	0.1 %w/w		Exact identifier — unii candidate 5 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION / INTRAVITREAL		6 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS	0.68 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Caramel	CARAMEL	T9D99G2B1R	SYRUP / ORAL	207 mg/5ml		Exact identifier — unii candidate 9 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRALESIONAL	0.9 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	TABLET, FILM COATED / ORAL		100 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / SUBCUTANEOUS		1486 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / EPIDURAL	0.9 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / ORAL		1126 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, FOR SOLUTION / INTRAPERITONEAL	226 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
Ammonium lauryl sulfate	AMMONIUM LAURYL SULFATE	Q7AO2R1M0B	EMULSION / TOPICAL	39.75 %w/w		Exact identifier — unii candidate 3 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SPRAY / NASAL		30 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SHAMPOO / TOPICAL		150 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / TOPICAL	0.86 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, EMULSION / INTRAVENOUS	0.62 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRAVITREAL	10 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	POWDER, FOR SUSPENSION / ORAL		98 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / AURICULAR (OTIC)		18 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR	226 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	POWDER / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION, LIPOSOMAL / EPIDURAL		11 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION / INTRAMUSCULAR		26 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / PARENTERAL		210 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / INTRA-ARTERIAL		278 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
Sodium Chloride	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / EPIDURAL		3535 mg	Exact identifier — unii candidate 134 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
41ac95c4-a5f8-4199-b354-067982deb899			a946566d-70f3-42a5-8e27-c1f67c5f40d5	2014-04-29	Warnings	Exact identifier spl id: 41ac95c4-a5f8-4199-b354-067982deb899 spl set id: a946566d-70f3-42a5-8e27-c1f67c5f40d5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.