Sulfur 8 Scalp Therapy Medicated Dandruff Control

Manufacturer
J. Strickland and Co.
Effective date
2025-11-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:25:56

Label at a glance#

ProductSulfur 8 Scalp Therapy Medicated Dandruff Control
Active ingredientPYRITHIONE ZINC
Label structure6 sections

Dosage and administration

shake well. for best results, use twice a week or as directed by a doctor wet hair, apply shampoo. lather, rinse & repeat

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc, 1%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

Controls scalp itching an flaking due to dandruff

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

seborrheic dermatitis that covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

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

Stop use and consult 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

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well.
  • for best results, use twice a week or as directed by a doctor
  • wet hair, apply shampoo. lather, rinse & repeat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Laureth Sulfate, Cocamidopropyl Betaine, PEG-3 Glyceryl Cocoate, Hydroxypropyl Methylcellulose, Sodium Cocoamphopropionate, Glycol Distearate, Glycol Stearate, Glycol, Magnesium Aluminum Silicate, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Triethylene Glycol, Magnesium Nitrate, Copper Sulfate, Citric Acid, Fragrance, Blue 1

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN4
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD4
209884zinc pyrithione 1 % Medicated ConditionerSY4
209884zinc pyrithione 1 % Medicated ShampooSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-036-00Sulfur 8 Scalp Therapy Medicated Dandruff Control280 mL in 1 BOTTLESHAMPOO, SUSPENSION2804

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-03612022-036-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
Sulfur 8 Scalp Therapy Medicated Dandruff ControlPYRITHIONE ZINCJ. Strickland and Co.96b26da0-d0d7-77ed-e053-2995a90a7a782025-11-07WarningsExact identifier
ndc (package): 12022-036-00
ndc (product): 12022-036
ndc11 (package): 12022003600
spl id: 430549de-fa5d-5929-e063-6394a90a9f9e
spl set id: 96b26da0-d0d7-77ed-e053-2995a90a7a78

Reported adverse events (FAERS/openFDA)#

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