FDA.reportPublic FDA data

Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner

Manufacturer
J. Strickland & Co.
Effective date
2023-10-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:57:10

Label at a glance#

ProductSulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner
Active ingredientSULFUR
Label structure8 sections

Dosage and administration

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

Sulfur, 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 occurs, rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallower, get medical help or call a poison control center at once.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to the affected area 1-4 times daily, or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Landin, Sorbitan Trioleate, Pclysorbate 81, Menthol, Mineral Oil, Fragrance, Amyl Cinnamal, Cinnamal, Citral, Citronellol, Geraniol, Limonene, Linalool

12022-017-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

017-00017-00

12022-017-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

017-01017-01

12022-017-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

017-02017-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
244368sulfur 2 % Topical OintmentPSN4
244368sulfur 0.02 MG/MG Topical OintmentSCD4
244368sulfur 2 % Topical OintmentSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-017-00Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner57 g in 1 JAROINTMENT574
12022-017-01Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner113 g in 1 JAROINTMENT1134
12022-017-02Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner205 g in 1 JAROINTMENT2054

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-017SULFUR 8 ORIGINAL ANTI-DANDRUFF HAIR AND SCALP CONDITIONER (SULFUR) OINTMENT [J. STRICKLAND & CO.]4Current NDC, Legacy NDC, 3 package rows20231021_eb1d6e9e-e7fd-478e-80c0-3a3f529682d7.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-01712022-017-00, 12022-017-01, 12022-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UIACT
LANOLIN7EV65EAW6HIACT
SORBITAN TRIOLEATEQE6F49RPJ1IACT
MENTHOLL7T10EIP3AIACT
MINERAL OILT5L8T28FGPIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
CINNAMALDEHYDESR60A3XG0FIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
SULFUR70FD1KFU70ACTIB

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 Original Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.eb1d6e9e-e7fd-478e-80c0-3a3f529682d72023-10-21WarningsExact identifier
ndc (package): 12022-017-01
ndc (package): 12022-017-00
ndc (package): 12022-017-02
ndc (product): 12022-017
ndc11 (package): 12022001700
ndc11 (package): 12022001701
ndc11 (package): 12022001702
spl id: 0834c116-5125-932d-e063-6394a90a13ac
spl set id: eb1d6e9e-e7fd-478e-80c0-3a3f529682d7

Reported adverse events (FAERS/openFDA)#

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