Dandruff Relief

Manufacturer
Rite Aid | Product Quest Mfg
Effective date
2018-06-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:02

Label at a glance#

ProductDandruff Relief daylogic
Active ingredientSalicylic Acid
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                    Purpose
Salicylic Acid 3%.................................... Psoriasis, Anti-dandruff,
                                                              and Seborrheic dermatitis

INDICATIONS & USAGE SECTION

Uses
Relieves and controls the following symptoms associated with
dandruff, seborrheic dermatitis and psoriasis
• scalp itching • flaking • irritation • redness • scaling

WARNINGS SECTION

Warnings
For external use only
Flammable - store away from fire or flame.
Allergy alert: do not use if allergic to salicylates or aspirin.
Consult a doctor before use
• if condition covers a large area of the body.
Stop use and consult a doctor
• if condition worsens or does not improve with regular use of
this product as directed.
When using this product
• avoid contact with eyes. If contact occurs, rinse eyes
thoroughly with water.
Keep out of the reach of children. If swallowed get medical
help or contact a Poison Control Center right away. If pregnant
or breast-feeding consult a health care professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions
• Apply to affected areas 1 to 4 times daily or as directed by a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Aloe Barbadensis Leaf Extract, Melaleuca Alternifolia (Tea Tree)
Leaf Oil, Menthol, Propylene Glycol, SD Alcohol 40-B,
Tocopheryl Acetate, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
251294salicylic acid 3 % Topical SolutionPSN1
251294salicylic acid 30 MG/ML Topical SolutionSCD1
251294salicylic acid 3 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-1237-32020-01-31C16284748780-19d75b9cf-cf6e-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1237-3Dandruff Reliefdaylogic74 mL in 1 BOTTLELIQUID741

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1237DANDRUFF RELIEF DAYLOGIC (SALICYLIC ACID 3.0%) LIQUID [RITE AID]1Legacy NDC, 1 package rows20180622_8d173e79-6459-4545-84fe-d9817a309b69.zip

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
11822-123711822-1237-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
146a62ff-ed84-44f7-a94e-f44003b08d068d173e79-6459-4545-84fe-d9817a309b692018-06-21WarningsExact identifier
spl id: 146a62ff-ed84-44f7-a94e-f44003b08d06
spl set id: 8d173e79-6459-4545-84fe-d9817a309b69

Reported adverse events (FAERS/openFDA)#

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