Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter Cream

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 Scalp Butter Cream
Active ingredientSULFUR, SALICYLIC ACID
Label structure6 sections

Dosage and administration

Apply a small amount to the scalp one to four times daily or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur, 5%

Salicylic Acid, 3%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

  • relieves the itching and scaling associated with dandruff

Warnings

WARNINGS SECTION

For external use only

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 as directed.
  • HAIR IS FLAMMABLE. Flammability is increased by product build-up. Keep hair away from sparks, flame, extreme heat or lit tobacco.

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

  • Apply a small amount to the scalp one to four times daily or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Mineral Oil, Tribehenin, Arachidyl Propionate, Polysorbate 20, Fragrance

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

33

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247682salicylic acid 3 % / sulfur 5 % Topical OintmentPSN3
247682salicylic acid 0.03 MG/MG / sulfur 0.05 MG/MG Topical OintmentSCD3
247682salicylic acid 3 % / sulfur 5 % Topical OintmentSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-035-00Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter Cream99 g in 1 JAROINTMENT993

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-035SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL SCALP BUTTER CREAM (SULFUR, SALICYLIC ACID) OINTMENT [J. STRICKLAND AND CO.]3Current NDC, Legacy NDC, 1 package rows20231021_96b26d20-d4d8-1bc3-e053-2995a90afec0.zip

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
12022-03512022-035-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 Control Scalp Butter CreamSULFUR, SALICYLIC ACIDJ. Strickland and Co.96b26d20-d4d8-1bc3-e053-2995a90afec02023-10-21WarningsExact identifier
ndc (package): 12022-035-00
ndc (product): 12022-035
ndc11 (package): 12022003500
spl id: 08350821-c7ca-6b7e-e063-6294a90ae838
spl set id: 96b26d20-d4d8-1bc3-e053-2995a90afec0

Reported adverse events (FAERS/openFDA)#

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