Quality Choice Therapeutic

Manufacturer
Chain Drug Marketing Association, Inc. | Medical Group Care LLC
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:28:09

Label at a glance#

ProductQuality Choice Therapeutic
Active ingredientSALICYLIC ACID
Label structure11 sections

Indications and uses

helps to stop the symptoms of these conditions and their recurrence: ▪ irritation ▪ itching ▪ redness ▪ flaking ▪ scaling

Dosage and administration

▪ wet hair, massage onto scalp, rinse and repeat if desired ▪ for best results use at least twice a week or as directed by a doctor ▪ for maximum dandruff control, use every time when you want to shampoo

Storage and handling

store away from direct sunlight, excessive heat, and freezing conditions

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 3%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff, Anti-psoriasis, and Anti-seborrheic dermatitis

Uses

INDICATIONS & USAGE SECTION

helps to stop the symptoms of these conditions and their recurrence: ▪ irritation ▪ itching ▪ redness ▪ flaking ▪ scaling

WARNINGS SECTION

Warnings  For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ wet hair, massage onto scalp, rinse and repeat if desired
▪ for best results use at least twice a week or as directed by a doctor
▪ for maximum dandruff control, use every time when you want to shampoo

Other information

STORAGE AND HANDLING SECTION

store away from direct sunlight, excessive heat, and freezing conditions

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl
Betaine, Hexylene Glycol, Sodium Citrate, Polyquaternium-22, Polyquaternium-10,
Citric Acid

OTC - QUESTIONS SECTION

Questions? +1-800-935-2362
You may also report serious side effects to this phone number.
Monday-Friday 9 AM - 5 PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205023salicylic acid 3 % Medicated ShampooPSN2
205023salicylic acid 30 MG/ML Medicated ShampooSCD2
205023salicylic acid 3 % Medicated ShampooSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-295-45Quality Choice Therapeutic133 mL in 1 BOTTLESHAMPOO1332
83324-295-45Quality Choice Therapeutic1 in 1 CARTONSHAMPOO12

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83324-29583324-295-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Quality Choice TherapeuticSALICYLIC ACIDChain Drug Marketing Association, Inc.46a009be-936d-ceb0-e063-6294a90a48512025-12-23WarningsExact identifier
ndc (package): 83324-295-45
ndc (product): 83324-295
ndc11 (package): 83324029545
spl id: 46a009c8-5470-bd2d-e063-6294a90aba0e
spl set id: 46a009be-936d-ceb0-e063-6294a90a4851

Reported adverse events (FAERS/openFDA)#

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