FDA.reportPublic FDA data

Sulfur 8 Anti-Dandruff Braid Spray

Manufacturer
J. Strickland & Co.
Effective date
2023-10-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:58:34

Label at a glance#

ProductSulfur 8 Anti-Dandruff Braid
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 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 consult 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

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, PEG-12 Dimethicone, Propylene Glycol, Sodium Hydroxide, Hydrolyzed Collagen, Disodium EDTA, Diazolidinyl Urea, Fragrance, Methylparaben, Propylparaben.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-021-0012022-021-00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
251577salicylic acid 2 % Topical SolutionPSN3
251577salicylic acid 20 MG/ML Topical SolutionSCD3
251577salicylic acid 2 % Topical SolutionSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-021-00Sulfur 8 Anti-Dandruff Braid356 mL in 1 BOTTLESOLUTION3563

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-021SULFUR 8 ANTI-DANDRUFF BRAID (SALICYLIC ACID) SOLUTION [J. STRICKLAND & CO.]3Current NDC, Legacy NDC, 1 package rows20231101_d240be47-8b86-4836-8407-c9ffe44628e8.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-02112022-021-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PEG-12 DIMETHICONEZEL54N6W95IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
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 Anti-Dandruff BraidSALICYLIC ACIDJ. Strickland & Co.d240be47-8b86-4836-8407-c9ffe44628e82023-10-21WarningsExact identifier
ndc (package): 12022-021-00
ndc (product): 12022-021
ndc11 (package): 12022002100
spl id: 08338925-6bc7-d723-e063-6394a90acfc8
spl set id: d240be47-8b86-4836-8407-c9ffe44628e8

Reported adverse events (FAERS/openFDA)#

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