Indications and uses
for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.
CVS Pharmacy
- Manufacturer
- CVS Pharmacy | Apollo Health and Beauty Care Inc.
- Effective date
- 2017-07-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:52:00
Label at a glance#
ProductCVS Pharmacy Maximum Strength Dandruff
Active ingredientSELENIUM SULFIDE
Label structure7 sections
Dosage and administration
Shake well, apply shampoo and rinse thoroughly. 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
Selenium Sulfide 1%
Purpose
Anti-dandruff/Anti-seborrheic dermatitis
Uses
for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.
Warnings
For external use only.
Ask a doctor before use if you have
seborrheic dermatitis in areas other than the scalp.
When using this product
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- for use on color or permed hair, rinse thoroughly.
Stop use and ask a doctor if
condition worsens or does not improve after regular use of this product as directed
Keep out of reach of children.
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- Shake well, apply shampoo and rinse thoroughly.
- for best results, use at least twice a week or as directed by a doctor.
Other information
store at room temperature.
Inactive ingredients
Water (Aqua), Sodium Laureth Sulfate, TEA-Lauryl Sulfate, Cocamidopropyl Betaine, Acrylates Copolymer, Citric Acid, Fragrance, Ammonium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Menthol, Sodium Hydroxide, Magnesium Aluminum Silicate, Hydroxypropyl Methylcellulose, Blue 1 (CI 42090), Red 33 (CI 17200).
Label Copy
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59779-719-11 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-185c-a910-e053-dadaa90a0b85 | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59779-719-11 | CVS PharmacyMaximum Strength Dandruff | 325 mL in 1 BOTTLE, PLASTIC | LIQUID | 325 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CVS Pharmacy Maximum Strength Dandruff
- Selenium Sulfide
- WATER
- SODIUM LAURETH SULFATE
- TRIETHANOLAMINE LAURYL SULFATE
- COCAMIDOPROPYL BETAINE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- CITRIC ACID MONOHYDRATE
- AMMONIUM CHLORIDE
- SODIUM HYDROXIDE
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- HYPROMELLOSES
- MAGNESIUM ALUMINUM SILICATE
- MENTHOL
- FD&C BLUE NO. 1
- D&C RED NO. 33
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59779-719 | 59779-719-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 2371023c-6df0-4c6a-bc99-a4e1ff9ad243 | 35dbb03f-150b-4540-a05c-4a2f33815b4a | 2017-07-19 | Warnings | 2371023c-6df0-4c6a-bc99-a4e1ff9ad243 35dbb03f-150b-4540-a05c-4a2f33815b4a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.