FDA.reportPublic FDA data

Daylogic Maximum Strength Dandruff

Manufacturer
RITE AID CORPORATION | APOLLO HEALTH AND BEAUTY CARE
Effective date
2016-02-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:56

Label at a glance#

ProductDaylogic Maximum Strength Dandruff
Active ingredientSELENIUM SULFIDE
Label structure6 sections

Indications and uses

helps prevent the recurrence of flaking, itching, irritation, scaling and redness associated with dandruff and seborrheic dermatitis.

Dosage and administration

shake well apply shampoo, rinse thoroughly for best results, use at least twice a week or as directed by a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Selenium Sulfide 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff, Anti-seborrheic dermatitis

Uses

INDICATIONS & USAGE SECTION

helps prevent the recurrence of flaking, itching, irritation, scaling and redness associated with dandruff and seborrheic dermatitis.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before using if you have

OTC - ASK DOCTOR SECTION

seborrheic dermatitis in areas other than the scalp.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • apply shampoo, rinse thoroughly
  • for best results, use at least twice a week or as directed by a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Glycol Distearate, Cocamide MEA, Ammonium Xylenesulfonate, Acrylates Copolymer, Sodium Hydroxide, Sodium Citrate, Fragrance (Parfum), Dimethicone, Cetyl Alcohol, Sodium Chloride, Citric Acid, Sodium Benzoate, Stearyl Alcohol, Disodium EDTA, Hydroxypropyl Methylcellulose, Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700).

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the labelImage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204642selenium sulfide 1 % Medicated ShampooPSN1
204642selenium sulfide 10 MG/ML Medicated ShampooSCD1
204642selenium sulfide 1 % Lotion ShampooSY1
204642selenium sulfide 1 % Medicated ShampooSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-6181-32020-01-31C16284748780-19d75b9d1-0e37-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-6181-3Daylogic Maximum Strength Dandruff420 mL in 1 BOTTLE, PLASTICLIQUID4201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-6181DAYLOGIC MAXIMUM STRENGTH DANDRUFF (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1Legacy NDC, 1 package rows20160211_b5e3550a-de63-42b5-90d3-5c23cca941c6.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-618111822-6181-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
SELENIUM SULFIDEZ69D9E381QACTIB
WATER059QF0KO0RIACT
AMMONIUM LAURETH-3 SULFATE896SJ235FNIACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
GLYCOL DISTEARATE13W7MDN21WIACT
COCO MONOETHANOLAMIDEC80684146DIACT
AMMONIUM XYLENESULFONATE4FZY6L6XCMIACT
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)74G4R6TH13IACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM CITRATE1Q73Q2JULRIACT
DIMETHICONE92RU3N3Y1OIACT
CETYL ALCOHOL936JST6JCNIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM BENZOATEOJ245FE5EUIACT
STEARYL ALCOHOL2KR89I4H1YIACT
EDETATE DISODIUM7FLD91C86KIACT
HYPROMELLOSES3NXW29V3WOIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C RED NO. 4X3W0AM1JLXIACT

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
506b2f61-d636-4e6d-825f-1c642a588ae0b5e3550a-de63-42b5-90d3-5c23cca941c62016-02-10WarningsExact identifier
spl id: 506b2f61-d636-4e6d-825f-1c642a588ae0
spl set id: b5e3550a-de63-42b5-90d3-5c23cca941c6

Reported adverse events (FAERS/openFDA)#

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