FDA.reportPublic FDA data

Daylogic 2in1 Dandruff Classic Clean

Manufacturer
Rite Aid Corporation | Apollo Health and Beautyc Care Inc. | Apollo Health and Beauty Care Inc.
Effective date
2017-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:33

Label at a glance#

ProductDaylogic 2in1 Dandruff Classic Clean
Active ingredientPYRITHIONE ZINC
Label structure6 sections

Indications and uses

to help prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

for maximum dandruff control, use every time you shampoo wet hair, massage onto scalp and rinse repeat if desired

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

to help prevent recurrence of flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with 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 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

  • for maximum dandruff control, use every time you shampoo
  • wet hair, massage onto scalp and rinse
  • repeat if desired

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Cocamide MEA, Glycol Distearate, Dimethicone, Acrylates Copolymer, Glycerin, Cocamidopropyl Betaine, Fragrance (Parfum), Laureth-4, Guar Hydroxypropyltrimonium Chloride, Sodium Hydroxide, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

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
209884zinc pyrithione 1 % Medicated ShampooPSN1
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD1
209884zinc pyrithione 1 % Medicated ConditionerSY1
209884zinc pyrithione 1 % Medicated ShampooSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130011822888059GTIN-13: 0011822888059
EAN-13: 0011822888059
GTIN-12: 011822888059
UPC-A: 011822888059
GTIN storage (14 digits): 00011822888059		20970L.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-4242-32020-01-31C16284748780-19d75b9d1-0678-f424-e053-dadaa90a57ceDrug Facts
11822-4242-42020-01-31C16284748780-19d75b9d1-0678-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-4242-3Daylogic 2in1 Dandruff Classic Clean695 mL in 1 BOTTLE, PLASTICLIQUID6951
11822-4242-4Daylogic 2in1 Dandruff Classic Clean420 mL in 1 BOTTLE, PLASTICLIQUID4201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-4242DAYLOGIC 2IN1 DANDRUFF CLASSIC CLEAN (PYRITHIONE ZINC) LIQUID [RITE AID CORPORATION]1Legacy NDC, 2 package rows20170410_6c3b6a46-2b44-430e-b4ef-994834e99c41.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-424211822-4242-3, 11822-4242-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
COCO MONOETHANOLAMIDEC80684146DIACT
GLYCOL DISTEARATE13W7MDN21WIACT
DIMETHICONE92RU3N3Y1OIACT
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE ANX76LV5T8JIACT
GLYCERINPDC6A3C0OXIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURETH-46HQ855798JIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT

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
8b2388de-6aba-4dc2-ae82-152debf06d8c6c3b6a46-2b44-430e-b4ef-994834e99c412017-04-10WarningsExact identifier
spl id: 8b2388de-6aba-4dc2-ae82-152debf06d8c
spl set id: 6c3b6a46-2b44-430e-b4ef-994834e99c41

Reported adverse events (FAERS/openFDA)#

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