Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Spray

Manufacturer
J. Strickland and Co.
Effective date
2023-10-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:57:07

Label at a glance#

ProductSulfur 8 Scalp Therapy Medicated Dandruff Control
Active ingredientSALICYLIC ACID
Label structure6 sections

Dosage and administration

Spray to apply to the affected area 1-4 times daily, or as directed by a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid, 2%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use:

INDICATIONS & USAGE SECTION

Controls scalp itching and flaking due to dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact, 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 at once.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray to apply to the affected area 1-4 times daily, or as directed by a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Sodium Hydroxide, PEG-40 Hydrogenate Castor Oil, PEG-12 Dimethicone, Propylene Glycol, Hydrolyzed Collagen, Diazolidinyl Urea, Disodium EDT, Methylparaben, Propylparaben, Ethylhexylglycerin, PEG-12 Alyl Ether, PEG-12, Butylene Glycol, Phenoxyethanol, Fragrance

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1048903salicylic acid 2 % Topical SprayPSN3
1048903salicylic acid 20 MG/ML Topical SpraySCD3
1048903salicylic acid 2 % Topical SpraySY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-032-00Sulfur 8 Scalp Therapy Medicated Dandruff Control355 mL in 1 BOTTLESPRAY3553

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-032SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL (SALICYLIC ACID) SPRAY [J. STRICKLAND AND CO.]3Current NDC, Legacy NDC, 1 package rows20231021_961ffab9-4e1b-83f3-e053-2a95a90af5fe.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-03212022-032-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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 ControlSALICYLIC ACIDJ. Strickland and Co.961ffab9-4e1b-83f3-e053-2a95a90af5fe2023-10-21WarningsExact identifier
ndc (package): 12022-032-00
ndc (product): 12022-032
ndc11 (package): 12022003200
spl id: 0834eb14-2e95-ef47-e063-6294a90ad922
spl set id: 961ffab9-4e1b-83f3-e053-2a95a90af5fe

Reported adverse events (FAERS/openFDA)#

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