Drug Facts

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC. | L'OREAL USA PRODUCTS, INC.
Effective date
2026-05-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:57:03

Label at a glance#

ProductCeraVe Anti-Dandruff Hydrating Conditioner
Active ingredientPYRITHIONE ZINC
Label structure11 sections

Dosage and administration

for best results use at least twice a week or as directed by a doctor use after CeraVe Anti-Dandruff Shampoo rinse and repeat if desired

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 0.5%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

helps prevents recurrence of scalp flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, rinse eyes throughly 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

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • for best results use at least twice a week or as directed by a doctor
  • use after CeraVe Anti-Dandruff Shampoo
  • rinse and repeat if desired

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetearyl alcohol, behentrimonium chloride, glycerin, PEG-180, amodimethicone, cetyl esters, ceramide NP, ceramide AP, ceramide EOP, carbomer, niacinamide, trideceth-6, triethyl citrate, sodium lauroyl lactylate, sodium hyaluronate, sodium polynaphthalenesulfonate, sodium chloride, sodium phosphate, cholesterol, phenoxyethanol, chlorhexidine dihydrochloride, disodium phosphate, isopropyl alcohol, propylene glycol, hydroxyethylcellulose, cetrimonium chloride, caprylyl glydol, xanthan gum, phytosphingosine, polysorbate 60, benzoic acid

Questions or comments?

OTC - QUESTIONS SECTION

Toll-free number 1-888-768-2915

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a labelcartoncartontubetube

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043014zinc pyrithione 0.5 % Medicated ConditionerPSN2
1043014zinc pyrithione 5 MG/ML Medicated ShampooSCD2
1043014zinc pyrithione 0.5 % Medicated ShampooSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-242-01CeraVe Anti-Dandruff Hydrating Conditioner266 mL in 1 TUBELIQUID2662
49967-242-02CeraVe Anti-Dandruff Hydrating Conditioner26 mL in 1 PACKETLIQUID262
49967-242-03CeraVe Anti-Dandruff Hydrating Conditioner15 in 1 PACKAGELIQUID152
49967-242-03CeraVe Anti-Dandruff Hydrating Conditioner29 mL in 1 TUBELIQUID292

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
49967-24249967-242-01, 49967-242-02, 49967-242-03

Ingredients#

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

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

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
CeraVe Anti-Dandruff Hydrating ConditionerPYRITHIONE ZINCL'Oreal USA Products Incd6a704df-edd8-4960-a088-246519e2aecf2026-05-12WarningsExact identifier
ndc (package): 49967-242-02
ndc (package): 49967-242-03
ndc (package): 49967-242-01
ndc (product): 49967-242
ndc11 (package): 49967024202
ndc11 (package): 49967024201
ndc11 (package): 49967024203
spl id: cb2a5460-c548-4ead-855e-5ff29a17ee37
spl set id: d6a704df-edd8-4960-a088-246519e2aecf

Reported adverse events (FAERS/openFDA)#

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