FDA.reportPublic FDA data

NDC-63148-212-12, CVS ANTI DANDRUFF SHAMPOO

Manufacturer
Apollo Health and Beauty Care
Effective date
2026-05-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:56:11

Label at a glance#

ProductCVS ANTI DANDRUFF
Active ingredientPYRITHIONE ZINC
Label structure7 sections

Indications and uses

Controls the symptoms of dandruff.

Dosage and administration

for best results, use at least twice weekly or as directed by the physician. Apply to wet skin and/or scalp and massage to form a lather. Leave lather on for few minutes. Rinse thoroughly and repeat if necessary.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc (1%)

Purpose

OTC - PURPOSE SECTION

Anti-dandruff.

Uses

INDICATIONS & USAGE SECTION

Controls the symptoms of dandruff.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rise eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsen 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 Comtrol Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • for best results, use at least twice weekly or as directed by the physician.
  • Apply to wet skin and/or scalp and massage to form a lather.
  • Leave lather on for few minutes.
  • Rinse thoroughly and repeat if necessary.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Cocamide MIPA, Glycol Stearate, Acrylates Copolymer, Amodimethicone, Tocopherol, Ceramide AP, Ceramide EOP, Ceramide NP, Niacinamide, Phytospingosine, Chlesterol, Sodium Hyaluronate, Polyquaternium-10, Carbomer, Cetrimonium Chloride, Trideceth-12, Coco-Betaine, Disodium Laureth Sulfosuccinate, Ethylhexylglycerin, Benzyl Alcohol, Sodium Hydroxide, Potato Starch Modified, PPG-5-Ceteth-20, Sodium Lauroyl Lactylate, Sodium Lauryl Sulfoacetate, Salicylic Acid, Xanthan Gum.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN3
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD3
209884zinc pyrithione 1 % Medicated ConditionerSY3
209884zinc pyrithione 1 % Medicated ShampooSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428169179GTIN-13: 0050428169179
EAN-13: 0050428169179
GTIN-12: 050428169179
UPC-A: 050428169179
GTIN storage (14 digits): 00050428169179		9493_06-26804_Sham_Ft.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-212-12CVS ANTI DANDRUFF355 mL in 1 BOTTLE, PLASTICSHAMPOO3553

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-21263148-212-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
COCO-BETAINE03DH2IZ3FYIACT
CERAMIDE 988KCS7120EIACT
WATER059QF0KO0RIACT
POLYQUATERNIUM-10 (400 CPS AT 2%)HB1401PQFSIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
SODIUM HYDROXIDE55X04QC32IIACT
COCAMIDE MIPA21X4Y0VTB1IACT
DISODIUM LAURETH SULFOSUCCINATED6DH1DTN7EIACT
GLYCOL STEARATE0324G66D0EIACT
SALICYLIC ACIDO414PZ4LPZIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
NIACINAMIDE25X51I8RD4IACT
CERAMIDE APF1X8L2B00JIACT
CERAMIDE NP4370DF050BIACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CHOLESTEROL97C5T2UQ7JIACT
TOCOPHEROLR0ZB2556P8IACT
PPG-5-CETETH-204AAN25P8P4IACT
TRIDECETH-12YFY3KG5Y7OIACT
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT
SODIUM LAURYL SULFOACETATED0Y70F2B9JIACT
AMODIMETHICONE (240 CST)VA5T401RWVIACT
CARBOMER0A5MM307FCIACT
XANTHAN GUMTTV12P4NEEIACT
STARCH, POTATO8I089SAH3TIACT
BENZYL ALCOHOLLKG8494WBHIACT
SODIUM HYALURONATEYSE9PPT4THIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-10-13monthly-update2026-06-03 17:38:45

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
CVS ANTI DANDRUFFPYRITHIONE ZINCApollo Health and Beauty Care3415172f-5a31-1085-e063-6394a90aabdc2026-05-03WarningsExact identifier
ndc (package): 63148-212-12
ndc (product): 63148-212
ndc11 (package): 63148021212
spl id: 50f20c2b-81f9-9fb6-e063-6394a90a0bfb
spl set id: 3415172f-5a31-1085-e063-6394a90aabdc

Reported adverse events (FAERS/openFDA)#

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