TopCare Dry Scalp Gentle Dandruff

Manufacturer: Topco Associates LLC | Apollo Health and Beauty Care Inc.
Effective date: 2019-09-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:00:39

Label at a glance#

ProductTopCare Dry Scalp Gentle Dandruff

Active ingredientPYRITHIONE ZINC

Label structure6 sections

Dosage and administration

for best results, use twice a week or as directed by a doctor wet hair, massage onto scalp and rinse. repeat if desired.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

to help prevent recurrence of flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

for best results, use twice a week or as directed by a doctor
wet hair, massage onto scalp and rinse.
repeat if desired.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Acrylates Copolymer, Glycol Distearate, Cocamidopropyl Betaine, Laureth-4, Fragrance (Parfum), Prunus Amygdalus Dulcis (Sweet Almond) Oil, Cocamide MEA, Sodium Hydroxide, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
209884	zinc pyrithione 1 % Medicated Shampoo	PSN	1
209884	zinc pyrithione 10 MG/ML Medicated Shampoo	SCD	1
209884	zinc pyrithione 1 % Medicated Conditioner	SY	1
209884	zinc pyrithione 1 % Medicated Shampoo	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
36800-796-14	2021-01-29	C162847	48780-1	ba0f9c33-1ef5-a910-e053-dadaa90a0b85	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
36800-796-14	TopCare Dry Scalp Gentle Dandruff	420 mL in 1 BOTTLE, PLASTIC	SHAMPOO	420		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
36800-796	TOPCARE DRY SCALP GENTLE DANDRUFF (PYRITHIONE ZINC) SHAMPOO [TOPCO ASSOCIATES LLC]	1	Legacy NDC, 1 package rows	20191001_ca91f0c5-55f3-49d2-9b67-0c7d18bc38e9.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

TopCare Dry Scalp Gentle Dandruff
Pyrithione Zinc
WATER
SODIUM LAURETH SULFATE
SODIUM CHLORIDE
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
GLYCOL DISTEARATE
COCAMIDOPROPYL BETAINE
LAURETH-4
ALMOND OIL
COCO MONOETHANOLAMIDE
SODIUM HYDROXIDE
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
36800-796	36800-796-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PYRITHIONE ZINC	R953O2RHZ5	ACTIB
WATER	059QF0KO0R	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)	74G4R6TH13	IACT
GLYCOL DISTEARATE	13W7MDN21W	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
LAURETH-4	6HQ855798J	IACT
ALMOND OIL	66YXD4DKO9	IACT
COCO MONOETHANOLAMIDE	C80684146D	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
EDETATE SODIUM	MP1J8420LU	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT

Source Document#

Source XML

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
88b3ab80-d762-4b2d-9fef-00cdc454418c			ca91f0c5-55f3-49d2-9b67-0c7d18bc38e9	2019-09-27	Warnings	Exact identifier spl id: 88b3ab80-d762-4b2d-9fef-00cdc454418c spl set id: ca91f0c5-55f3-49d2-9b67-0c7d18bc38e9

Reported adverse events (FAERS/openFDA)#

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