FDA.reportPublic FDA data

2 in 1 Dandruff

Manufacturer
Retail Business Services, LLC | Nice-Pak Products, LLC
Effective date
2026-02-06
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:37:23

Label at a glance#

Product2 in 1 Dandruff
Active ingredientPYRITHIONE ZINC
Label structure12 sections

Dosage and administration

shake well for maximum dandruff control, use every time you shampoo wet hair, massage onto scalp, rinse, repeat if desired for best results use at least twice a week or as directed by a doctor

Label contents#

Full prescribing information#

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Procter & Gamble, the owner of the registered trademark Head & Shoulders ® Coconut 2 in 1 Dandruff Shampoo & Conditioner.

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

helps prevent recurrence of flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into 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 as directed

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • for maximum dandruff control, use every time you shampoo
  • wet hair, massage onto scalp, rinse, repeat if desired
  • for best results use at least twice a week or as directed by a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, cocamidopropyl betaine, sodium xylenesulfonate, fragrance, amodimethicone, guar hydroxypropyltrimonium chloride, sodium benzoate, propylene glycol, citric acid, magnesium carbonate hydroxide, Cocos nucifera (coconut) fruit extract, hexyl cinnamal, benzyl salicylate, limonene, methylchloroisothiazolinone, methylisothiazolinone

Adverse Reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC

SALISBURY, NC 28147

For product questions or concerns, contact us at 1-833-922-3872

Quality guaranteed or your money back.

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 72476-362-02

CAREone ®

Compare to Head & Shoulders ®Coconut 2 in 1 Dandruff Shampoo + Conditioner*

2 IN 1 Coconut Dandruff Shampoo & Conditioner

Dandruff Fighting Formula

  • Helps promote healthy hair and scalp
  • Pyrithione Zinc

12.5 FL OZ (370 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN8
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD8
209884zinc pyrithione 1 % Medicated ConditionerSY8
209884zinc pyrithione 1 % Medicated ShampooSY8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0021371BAmm02.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72476-362-012 in 1 Dandruff420 mL in 1 BOTTLE, PLASTICSHAMPOO4208
72476-362-022 in 1 Dandruff370 mL in 1 BOTTLE, PLASTICSHAMPOO3708

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72476-36272476-362-01, 72476-362-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM CHLORIDE451W47IQ8XIACT
ZINC CARBONATEEQR32Y7H0MIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM XYLENESULFONATEG4LZF950URIACT
AMODIMETHICONE (800 CST)363Z2T48P7IACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
SODIUM BENZOATEOJ245FE5EUIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
MAGNESIUM CARBONATE HYDROXIDEYQO029V1L4IACT
COCONUT3RT3536DHYIACT
HEXYL CINNAMATE532UJ0Y6RIIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
LIMONENE, (+)-GFD7C86Q1WIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-11-13monthly-update2026-06-03 17:39:59

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2 in 1 DandruffPYRITHIONE ZINCRetail Business Services, LLCec9d36ae-cf4e-4841-a13e-5cb0fe64c4fa2026-02-06Warnings, Adverse reactionsExact identifier
ndc (package): 72476-362-02
ndc (package): 72476-362-01
ndc (product): 72476-362
ndc11 (package): 72476036201
ndc11 (package): 72476036202
spl id: 4a2b83a8-e257-699d-e063-6394a90aaf5e
spl set id: ec9d36ae-cf4e-4841-a13e-5cb0fe64c4fa

Reported adverse events (FAERS/openFDA)#

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