63148-208, CVS Dandruff Shampoo and Conditioner- Men's Sport

Manufacturer
Apollo Health and Beauty Care
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:56:37

Label at a glance#

ProductMens Sport
Active ingredientPYRITHIONE ZINC
Label structure7 sections

Indications and uses

Helps prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

Apply a generous amount to wet hair, massage onto scalp and work evenly to the ends. Leave on for 3-5 minutes. Rinse throughly. For best results use at least twice a week or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

For External Use only

When using the 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

  • Apply a generous amount to wet hair, massage onto scalp and work evenly to the ends.
  • Leave on for 3-5 minutes.
  • Rinse throughly.
  • For best results use at least twice a week or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

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 ShampooPSN6
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD6
209884zinc pyrithione 1 % Medicated ConditionerSY6
209884zinc pyrithione 1 % Medicated ShampooSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428101605GTIN-13: 0050428101605
EAN-13: 0050428101605
GTIN-12: 050428101605
UPC-A: 050428101605
GTIN storage (14 digits): 00050428101605
06-26266V1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-208-20Mens Sport612 mL in 1 BOTTLE, PLASTICSHAMPOO6126

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
63148-20863148-208-20

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-10monthly-update2026-06-03 17:39:42
22024-11-14full-release2026-06-01 00:37:18

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
Mens SportPYRITHIONE ZINCApollo Health and Beauty Care1d1203ea-9994-31bb-e063-6394a90a9ec82026-05-08WarningsExact identifier
ndc (package): 63148-208-20
ndc (product): 63148-208
ndc11 (package): 63148020820
spl id: 5151f614-90fc-e411-e063-6394a90ac998
spl set id: 1d1203ea-9994-31bb-e063-6394a90a9ec8

Reported adverse events (FAERS/openFDA)#

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