OCEAN BREEZE 2 IN 1 DANDRUFF

Manufacturer: SUPERVALU INC
Effective date: 2010-07-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:25:45

Label at a glance#

ProductOCEAN BREEZE 2 IN 1 DANDRUFF SEA MINERAL SCENT

Active ingredientPYRITHIONE ZINC

Label structure7 sections

Indications and uses

HELPS 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 DESIRE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

PYRITHIONE ZINC 1%

PURPOSE

OTC - PURPOSE SECTION

ANTI-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 THROUGHLY 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 POISON CONTROL CENTER IMMEDIATELY.

Uses

INDICATIONS & USAGE SECTION

HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF

Directions

DOSAGE & ADMINISTRATION SECTION

FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRE.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Zinc Carbonate, Glycol Distearate, Fragrance (Parfum), Dimethicone, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Menthol, PEG-7M, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Sea Salt, Fucus Vesiculosus Extract, Benzyl Alcohol, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Xylene Sulfonate, Blue 1 (CI 42090), Yellow 5 (CI 19140)

PACKAGE FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

14OZ Front and Back Labels: eq14.jpg14 OZ FRONT AND BACK LABELS

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
41163-420-14	2020-01-31	C162847	48780-1	9d75b9d0-5d55-f424-e053-dadaa90a57ce	BACK LABEL - DRUG FACTS BOX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41163-420-14	OCEAN BREEZE 2 IN 1 DANDRUFFSEA MINERAL SCENT	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
41163-420	OCEAN BREEZE 2 IN 1 DANDRUFF SEA MINERAL SCENT (PYRITHIONE ZINC) SHAMPOO [SUPERVALU INC]	1	Legacy NDC, 1 package rows	20100903_aca69d6f-dafc-40d9-a5ce-3fb1279143ab.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
PYRITHIONE ZINC	ACTIVE INGREDIENT	R953O2RHZ5	1
PYRITHIONE ZINC	ACTIVE MOIETY	R953O2RHZ5	1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

OCEAN BREEZE 2 IN 1 DANDRUFF SEA MINERAL SCENT
PYRITHIONE ZINC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41163-420	41163-420-14

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
PYRITHIONE ZINC	R953O2RHZ5	ACTIB

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
e961aac9-c831-49b1-ba12-71389e191175			aca69d6f-dafc-40d9-a5ce-3fb1279143ab	2010-07-01	Warnings	Exact identifier spl id: e961aac9-c831-49b1-ba12-71389e191175 spl set id: aca69d6f-dafc-40d9-a5ce-3fb1279143ab

Reported adverse events (FAERS/openFDA)#

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