Head and Shoulders Bare Minimal Ingredients

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:29:42

Label at a glance#

ProductHead and Shoulders Bare Minimal Ingredients
Active ingredientPYRITHIONE ZINC
Label structure10 sections

Indications and uses

fights recurrence of the symptoms of dandruff.

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

fights recurrence of the symptoms of 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.
  • shake before use, wet hair, massage onto scalp, rinse, repeat if desired.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, lauramidopropyl betaine, sodium cocoyl isethionate, fragrance, acrylates copolymer, polyquaternium-10, sodium benzoate, citric acid

Questions (or comments)?

OTC - QUESTIONS SECTION

1-800-723-9569

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 400 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

head &
shoulders ®
PYRITHIONE ZINC DANDRUFF SHAMPOO

BARE

MINIMAL INGREDIENTS SHAMPOO

PURE CLEAN

0% SULFATES

DYES

SILICONES

13.5 FL OZ
(400 mL)

HSHS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043244head & shoulders 1 % Medicated ShampooPSN3
209884zinc pyrithione 1 % Medicated ShampooPSN3
1043244zinc pyrithione 10 MG/ML Medicated Shampoo [Head & Shoulders]SBD3
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD3
1043244Head & Shoulders 1 % Medicated ShampooSY3
1043244Head & Shoulders 10 MG/ML Medicated ShampooSY3
209884zinc pyrithione 1 % Medicated ConditionerSY3
209884zinc pyrithione 1 % Medicated ShampooSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69423-721-40Head and Shoulders Bare Minimal Ingredients350 mL in 1 BOTTLE, PLASTICSHAMPOO3503

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-72169423-721-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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 Bare Minimal IngredientsPYRITHIONE ZINCThe Procter & Gamble Manufacturing Company003c585f-9fda-c86e-e063-6394a90ae3772025-12-31WarningsExact identifier
ndc (package): 69423-721-40
ndc (product): 69423-721
ndc11 (package): 69423072140
spl id: 47461ad3-a11d-2a11-e063-6294a90a0f8f
spl set id: 003c585f-9fda-c86e-e063-6394a90ae377

Reported adverse events (FAERS/openFDA)#

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