Indications and uses
to help prevent recurrence of flaking and itching associated with dandruff.
P.O.V. Dry Scalp Dandruff
- Manufacturer
- Apollo Health and Beauty Care Inc.
- Effective date
- 2017-11-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:53:04
Label at a glance#
ProductP.O.V. Dry Scalp Dandruff
Active ingredientPYRITHIONE ZINC
Label structure7 sections
Dosage and administration
Wet hair and apply evenly to scalp, massaging gently. Rinse thoroughly. Repeat as needed. For best results, use at least twice a week or as directed by a doctor.
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Pyrithione Zinc 1%
Purpose
Anti-dandruff
Uses
to help prevent recurrence of flaking and itching associated with dandruff.
Warnings
For external use only.
When using this product
avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if
condition worsens or does not improve with 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
Wet hair and apply evenly to scalp, massaging gently. Rinse thoroughly. Repeat as needed. For best results, use at least twice a week or as directed by a doctor.
Inactive ingredients
Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Cocamidopropyl Betaine, Acrylates Copolymer, Laureth-4, Fragrance (Parfum), Dimethicone, Cocamide MEA, Guar Hydroxypropyltrimonium Chloride, Sodim Hydroxide, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.
Questions or comments?
1-866-695-3030
Label Copy
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63148-416-24 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4136-111a-e063-dadaa90a10e2 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63148-416-24 | P.O.V. Dry Scalp Dandruff | 701 mL in 1 BOTTLE, PLASTIC | SHAMPOO | 701 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- P.O.V. Dry Scalp Dandruff
- Pyrithione Zinc
- WATER
- SODIUM LAURETH SULFATE
- SODIUM CHLORIDE
- GLYCOL DISTEARATE
- COCAMIDOPROPYL BETAINE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- LAURETH-4
- DIMETHICONE
- COCO MONOETHANOLAMIDE
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)
- SODIUM HYDROXIDE
- EDETATE SODIUM
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63148-416 | 63148-416-24 |
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 |
|---|---|---|---|---|---|---|
| 8486bf4c-e409-42b5-a78d-cabdcd5e8a67 | cc302387-e156-40b3-b940-e368826aee9d | 2017-11-21 | Warnings | 8486bf4c-e409-42b5-a78d-cabdcd5e8a67 cc302387-e156-40b3-b940-e368826aee9d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.