EQUATE CLASSIC SPICE 2 IN 1 DANDRUFF

Manufacturer: WAL-MART STORES INC | APOLLO HEALTH AND BEAUTY CARE
Effective date: 2016-02-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:45:02

Label at a glance#

ProductEQUATE CLASSIC SPICE 2 IN 1 DANDRUFF

Active ingredientPYRITHIONE ZINC

Label structure6 sections

Indications and uses

to help prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

for maximum dandruff control, use every time you shampoo 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

Anti-dandruff

Uses

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 maximum dandruff control, use every time you shampoo
wet hair, massage onto scalp and rinse
repeat if desired

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Glycol Distearate, Zinc Carbonate, Sodium Chloride, Sodium Xylenesulfonate, Cocamidopropyl Betaine, Dimethicone, Fragrance (Parfum), Sodium Benzoate, Guar Hydroxypropyltrimonium Chloride, Magnesium Carbonate Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

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
49035-432-13	2020-01-31	C162847	48780-1	9d75b9d0-fb35-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-432-13	EQUATE CLASSIC SPICE 2 IN 1 DANDRUFF	399 mL in 1 BOTTLE, PLASTIC	SHAMPOO	399		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-432	EQUATE CLASSIC SPICE 2 IN 1 DANDRUFF (PYRITHIONE ZINC) SHAMPOO [WAL-MART STORES INC]	1	Legacy NDC, 1 package rows	20160218_76edd3a2-6cce-43ce-adaf-e3acceb62242.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

EQUATE CLASSIC SPICE 2 IN 1 DANDRUFF
PYRITHIONE ZINC
WATER
SODIUM LAURYL SULFATE
SODIUM LAURETH-3 SULFATE
GLYCOL DISTEARATE
ZINC CARBONATE
SODIUM CHLORIDE
SODIUM XYLENESULFONATE
COCAMIDOPROPYL BETAINE
DIMETHICONE
SODIUM BENZOATE
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)
MAGNESIUM CARBONATE HYDROXIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C BLUE NO. 1
D&C RED NO. 33

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49035-432	49035-432-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PYRITHIONE ZINC	R953O2RHZ5	ACTIB
WATER	059QF0KO0R	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SODIUM LAURETH-3 SULFATE	BPV390UAP0	IACT
GLYCOL DISTEARATE	13W7MDN21W	IACT
ZINC CARBONATE	EQR32Y7H0M	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM XYLENESULFONATE	G4LZF950UR	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
DIMETHICONE	92RU3N3Y1O	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)	B16G315W7A	IACT
MAGNESIUM CARBONATE HYDROXIDE	YQO029V1L4	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
D&C RED NO. 33	9DBA0SBB0L	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
eaddba37-0f37-43bd-ae43-c3d68a2b7602			76edd3a2-6cce-43ce-adaf-e3acceb62242	2016-02-17	Warnings	Exact identifier spl id: eaddba37-0f37-43bd-ae43-c3d68a2b7602 spl set id: 76edd3a2-6cce-43ce-adaf-e3acceb62242

Reported adverse events (FAERS/openFDA)#

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