FDA.reportPublic FDA data

Sulfur 8 Fresh 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 23:57:06

Label at a glance#

ProductSulfur 8 Fresh Anti-Dandruff Hair and Scalp Conditioner
Active ingredientSALICYLIC ACID
Label structure6 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

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

  • 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

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

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Cetyl Alcohol, Paraffin, Butyrospermum Parkii (Shea Butter), Theobromo Grandiflorum Seed Butter, Mineral Oil, Menthol, Fragrance, Sorbitan Trioleate, Allantion, Polysorbate 81

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

022-026022-026

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
251400salicylic acid 2 % Topical OintmentPSN4
251400salicylic acid 0.02 MG/MG Topical OintmentSCD4
251400salicylic acid 2 % Topical OintmentSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-026-00Sulfur 8 Fresh Anti-Dandruff Hair and Scalp Conditioner108 g in 1 JAROINTMENT1084

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-026SULFUR 8 FRESH ANTI-DANDRUFF HAIR AND SCALP CONDITIONER (SALICYLIC ACID) OINTMENT [J. STRICKLAND & CO.]4Current NDC, Legacy NDC, 1 package rows20231021_27b6276a-eaa0-4fb7-996c-53e8c2868091.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-02612022-026-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UIACT
CETYL ALCOHOL936JST6JCNIACT
PARAFFINI9O0E3H2ZEIACT
SHEA BUTTERK49155WL9YIACT
THEOBROMA GRANDIFLORUM SEED BUTTERI711F13FXMIACT
MINERAL OILT5L8T28FGPIACT
MENTHOLL7T10EIP3AIACT
SORBITAN TRIOLEATEQE6F49RPJ1IACT
ALLANTOIN344S277G0ZIACT
POLYSORBATE 812MSF640LWMIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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 Fresh Anti-Dandruff Hair and Scalp ConditionerSALICYLIC ACIDJ. Strickland & Co.27b6276a-eaa0-4fb7-996c-53e8c28680912023-10-21WarningsExact identifier
ndc (package): 12022-026-00
ndc (product): 12022-026
ndc11 (package): 12022002600
spl id: 0834cc0a-a4e6-be61-e063-6294a90a456b
spl set id: 27b6276a-eaa0-4fb7-996c-53e8c2868091

Reported adverse events (FAERS/openFDA)#

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