CONTROL Anti-Dandruff

Manufacturer
AG Hair Ltd
Effective date
2023-06-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:30:02

Label at a glance#

ProductCONTROL Anti-Dandruff
Active ingredientPYRITHIONE ZINC
Label structure7 sections

Indications and uses

helps prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

• Apply shampoo and work into a lather. • Massage into scalp, leave on for 3-5 minutes. • Rinse thoroughly for best results. • Use at least twice per week until dandruff is eliminated, or as directed by a pharmacist/physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 2%

PURPOSE:

OTC - PURPOSE SECTION

Anti-Dandruff

USES:

INDICATIONS & USAGE SECTION

helps prevent recurrence of flaking and itching associated with dandruff.

WARNING:

WARNINGS SECTION

for external use only.

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

• Avoid contact with eyes. if contact occurs, rinse eyes thoroughly 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

• Apply shampoo and work into a lather.
• Massage into scalp, leave on for 3-5 minutes.
• Rinse thoroughly for best results.
• Use at least twice per week until dandruff is eliminated, or as directed by a pharmacist/physician.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Aqua (Water/Eau), Sodium Lauroyl Sarcosinate, Sodium Taurine Cocoyl Methyltaurate, Coco-Betaine, Sodium Cocoyl Isethionate, Cocamidopropyl Hydroxysultaine, Sodium Cocoyl Alaninate, Acrylates Copolymer, Cocamidopropyl Betaine, PEG/PPG-120/10 Trimethylolpropane Trioleate, Coco-Glucoside, Hydrogenated Castor Oil, Propanediol, Laureth-2, Parfum (Fragrance), Sodium Benzoate, Potassium Sorbate, Polyquaternium-10, Menthol, Tocopheryl Acetate, Glycerin, Limonene, Panthenol, Sodium PCA, Benzyl Benzoate, Hydrolyzed Pea Protein, Hydrolyzed Vegetable Protein, Linalool, Cucumis Sativus (Cucumber) Fruit Extract, Aloe Barbadensis Leaf Extract.

QUESTIONS (OR COMMENTS)?

OTC - QUESTIONS SECTION

1-866-924-4247

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46324-242246324-2422-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
fe1d0a62-851f-25a8-e053-6394a90a759737865272-70ed-4f39-bbc5-eb3839ae27c02023-06-14WarningsExact identifier
spl id: fe1d0a62-851f-25a8-e053-6394a90a7597
spl set id: 37865272-70ed-4f39-bbc5-eb3839ae27c0

Reported adverse events (FAERS/openFDA)#

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