FDA.reportPublic FDA data

Sulfur 8 Light 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 23:57:09

Label at a glance#

ProductSulfur 8 Light 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 Ingredients

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

  • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • a gradual blue-black darking of the skin occurs
  • irritation becomes severe
  • no improvement is seen after 3 months

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, Lanolin, Mineral Oil, Menthol, Fragrance, Yellow 11.

12022-018-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

018-00018-00

12022-018-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

018-01018-01

12022-018-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

018-02018-02

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
12022-018-00Sulfur 8 Light Anti-Dandruff Hair and Scalp Conditioner57 g in 1 JAROINTMENT574
12022-018-01Sulfur 8 Light Anti-Dandruff Hair and Scalp Conditioner113 g in 1 JAROINTMENT1134
12022-018-02Sulfur 8 Light Anti-Dandruff Hair and Scalp Conditioner205 g in 1 JAROINTMENT2054

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-018SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER (SULFUR) OINTMENT [J. STRICKLAND & CO.]4Current NDC, Legacy NDC, 3 package rows20231021_d8f9afe8-bc44-41be-806b-b77d2def0fb0.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-01812022-018-00, 12022-018-01, 12022-018-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UIACT
LANOLIN7EV65EAW6HIACT
MINERAL OILT5L8T28FGPIACT
MENTHOLL7T10EIP3AIACT
D&C YELLOW NO. 1144F3HYL954IACT
SULFUR70FD1KFU70ACTIB

Source Document#

Source XML · Source PDF

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 Light Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.d8f9afe8-bc44-41be-806b-b77d2def0fb02023-10-21WarningsExact identifier
ndc (package): 12022-018-01
ndc (package): 12022-018-02
ndc (package): 12022-018-00
ndc (product): 12022-018
ndc11 (package): 12022001802
ndc11 (package): 12022001801
ndc11 (package): 12022001800
spl id: 0833fc64-f83f-f3b0-e063-6294a90aeec1
spl set id: d8f9afe8-bc44-41be-806b-b77d2def0fb0

Reported adverse events (FAERS/openFDA)#

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