Careone Medicated Dandruff

Manufacturer
Spa Dent Inc | Apollo Health and Beauty Care
Effective date
2021-07-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:38

Label at a glance#

ProductCareone Medicated Dandruff
Active ingredientSELENIUM SULFIDE
Label structure9 sections

Indications and uses

for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.

Dosage and administration

Shake well, wet hair, massage onto scalp and rinse. For best results, use at least twice a week or as directed by a doctor. 

Storage and handling

Store at room temperature

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

for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have seborrheic dermatitis in areas other than the scalp.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • For use on color treated or permed hair, rinse thoroughly.

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, wet hair, massage onto scalp and rinse.
  • For best results, use at least twice a week or as directed by a doctor. 

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, TEA-Lauryl Sulfate, Cocamidopropyl Betaine, Acrylates Copolymer, Citric Acid, Fragrance (Parfum), Ammonium Chloride, Menthol, Sodium Hydroxide, Magnesium Aluminium Silicate, Hydroxypropyl Methylcellulose, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (Cl 42090), Red 33 (Cl 17200).

Questions or comments ?

OTC - QUESTIONS SECTION

1-877-846-9949

PDP03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP03PDP03

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79147-02579147-025-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
92cf85a7-4fbd-471d-b268-0e23ac4517afa39f93b4-2263-472a-a547-7a8deb81dd3a2021-07-26WarningsExact identifier
spl id: 92cf85a7-4fbd-471d-b268-0e23ac4517af
spl set id: a39f93b4-2263-472a-a547-7a8deb81dd3a

Reported adverse events (FAERS/openFDA)#

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