Dosage and administration
Directions - shake well. Wet hair. Massage onto scalp. Rinse. Repeat if desired. - for best results use at least twice a week or as directed by a doctor. - for maximum dandruff control, use every time you shampoo.
Royal Dandruff Dry Scalp
- Manufacturer
- Mission Series Inc. dba Prestige Beauty Care
- Effective date
- 2020-05-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:13:34
Label at a glance#
ProductRoyal Dandruff Dry Scalp
Active ingredientPYRITHIONE ZINC
Label structure11 sections
Label contents#
Full prescribing information#
Active Ingredient
Active Ingredient - Pyrithione Zinc 1%
Purpose
Purpose
Anti-dandruff
Use
Use - helps protect the scalp's natural moisture balance and gives you great looking hair.
Warnings
Warnings - For external use only.
When using this product
When using this product
- do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Stop Use
Stop use and ask a doctor if
- condition worsens or does not improve after regular use as directed.
Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions
- shake well. Wet hair. Massage onto scalp. Rinse. Repeat if desired.
- for best results use at least twice a week or as directed by a doctor.
- for maximum dandruff control, use every time you shampoo.
Inactive Ingredients
Inactive Ingredients - Water, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Amodimethicone, Sodium Chloride, Glycol Distearate, Cetyl Alcohol, Cocamide MEA, Fragrance, Polyquaternium-10, Sodium Citrate, Hydrogentated Polydecene, Sodium Benzoate, Trideceth-12, Cetrimonium Chloride, Citric Acid, Ammonium Xylenesulfonate, FD&C Blue No. 1, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone.
Distributed By
Distributed By:
PRESTIGE BEAUTY CARE
1585 West Mission Blvd.
Pomona, CA 91766
Made in China
Royal Dandruff Shampoo Dry Scalp
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73597-009-10 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-582b-a426-e053-dadaa90af4c2 | Royal Dandruff Dry Scalp |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73597-009-10 | Royal Dandruff Dry Scalp | 273.06 g in 1 BOTTLE | SHAMPOO | 273.06 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Royal Dandruff Dry Scalp
- Pyrithione Zinc
- AMMONIUM LAURETH-2 SULFATE
- AMODIMETHICONE (800 CST)
- POLYQUATERNIUM-10 (10000 MPA.S AT 2%)
- SODIUM CITRATE
- CITRIC ACID MONOHYDRATE
- SODIUM BENZOATE
- TRIDECETH-12
- FD&C BLUE NO. 1
- WATER
- BENZYL ALCOHOL
- METHYLISOTHIAZOLINONE
- AMMONIUM LAURYL SULFATE
- HYDROGENATED POLYDECENE TYPE I
- SODIUM CHLORIDE
- CETYL ALCOHOL
- COCO MONOETHANOLAMIDE
- CETRIMONIUM CHLORIDE
- GLYCOL DISTEARATE
- AMMONIUM XYLENESULFONATE
- METHYLCHLOROISOTHIAZOLINONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73597-009 | 73597-009-10 |
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 |
|---|---|---|---|---|---|---|
| a56722e7-3369-0ed4-e053-2a95a90ad3c7 | a5672324-f421-0a4d-e053-2a95a90a6f34 | 2020-05-18 | Warnings | a56722e7-3369-0ed4-e053-2a95a90ad3c7 a5672324-f421-0a4d-e053-2a95a90a6f34 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.