Head and Shoulders Supreme Detox and Hydrate Conditioner

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:26:53

Label at a glance#

ProductHead and Shoulders Supreme Detox and Hydrate Conditioner
Active ingredientPYRITHIONE ZINC
Label structure10 sections

Indications and uses

helps prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

for best results use at least twice a week or as directed by a doctor. apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 0.5%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • for best results use at least twice a week or as directed by a doctor.
  • apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, stearyl alcohol, behentrimonium chloride, cetyl alcohol, argania spinosa kernel oil, zea mays (corn) silk extract, cocos nucifera (coconut) fruit extract, fragrance, phenoxyethanol, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone

Questions (or comments)?

OTC - QUESTIONS SECTION

1-800-723-9569

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 247 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

head &
shoulders ®

PYRITHION ZINC DANDRUFF

SCALP & HAIR CONDITIONER

SUPREME

DETOX &

HYDRATE

WITH ARGAN OIL & COCONUT WATER

FREE FROM

SULFATES

PARABENS

PHTHALATES

DYES

9.4 FL OZ
(278 mL)

HSHS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1044465head & shoulders 0.5 % Medicated ShampooPSN8
1043014zinc pyrithione 0.5 % Medicated ConditionerPSN8
1044465zinc pyrithione 5 MG/ML Medicated Shampoo [Head & Shoulders]SBD8
1043014zinc pyrithione 5 MG/ML Medicated ShampooSCD8
1044465Head & Shoulders 0.5 % ConditionerSY8
1044465Head & Shoulders 5 MG/ML Medicated ShampooSY8
1043014zinc pyrithione 0.5 % Medicated ShampooSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69423-347-27Head and Shoulders Supreme Detox and Hydrate Conditioner278 mL in 1 TUBELOTION2788

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-34769423-347-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Head and Shoulders Supreme Detox and Hydrate ConditionerPYRITHIONE ZINCThe Procter & Gamble Manufacturing Company86ab72bc-4e9d-0075-e053-2a91aa0a11352025-12-18WarningsExact identifier
ndc (package): 69423-347-27
ndc (product): 69423-347
ndc11 (package): 69423034727
spl id: 4640c427-fbac-1ff7-e063-6394a90a4e63
spl set id: 86ab72bc-4e9d-0075-e053-2a91aa0a1135

Reported adverse events (FAERS/openFDA)#

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