RemedyDandruffShampooTreatment

Manufacturer
Naturich Cosmetique Labs
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:38:16

Label at a glance#

ProductRemedyDandruffShampooTreatment
Active ingredientPYRITHIONE ZINC
Label structure11 sections

Indications and uses

• Helps prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

Directions • Use daily, or as directed by a doctor for maximum dandruff control. • Massage onto wet scalp and hair, using scalp massager, if preferred. Wait 3 minutes before rinsing for best results.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1.00% ..............................................................................Anti-Dandruff

Purpose:

OTC - PURPOSE SECTION

Anti-Dandruff

When Using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Warnings

WARNINGS SECTION

• For external use only.

Stop Use

OTC - STOP USE SECTION

Stop use and ask doctor if 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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

USES

INDICATIONS & USAGE SECTION

• Helps prevent recurrence of flaking and itching associated with dandruff.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
• Use daily, or as directed by a doctor for maximum dandruff control.
• Massage onto wet scalp and hair, using scalp massager, if preferred. Wait 3 minutes before rinsing for best results.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Decyl Glucoside, Cocamidopropyl Betaine, Propanediol, Dimethicone, Lauryl Glucoside, Glyceryl Stearate, Coco-Betaine, Jojoba Esters, Glycerin, Camellia Sinensis Leaf Extract, Serenoa Serrulata Fruit Extract, Trifolium Pratense Flower Extract, Hydrolyzed Quinoa, Mentha Arvensis Leaf Oil, Mentha Piperita (Peppermint) Oil, Glycol Distearate, Capryloyl Glycine, Laureth-4, Niacinamide, Xylitol, Xylitylglucoside, Anhydroxylitol, Menthol, Coco Nucifera (Coconut) Shell Powder, Polyacrylate Crosspolymer-6, Hexylene Glycol, Xanthan Gum, PEG-40 Castor Oil, Fragrance, Phenoxyethanol, Benzyl Alcohol, CI 42090 Acid Blue 9.

Questions?

OTC - QUESTIONS SECTION

Questions? 877-690-6466

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ACTIIVACTIIV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72496-1038-1RemedyDandruffShampooTreatment207 mL in 1 BOTTLESHAMPOO2074
72496-1038-2RemedyDandruffShampooTreatment247 mL in 1 BOTTLE, PUMPSHAMPOO2474

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72496-103872496-1038-1, 72496-1038-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-03-12full-release2026-06-01 00:09:40

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
RemedyDandruffShampooTreatmentACTIIV REMEDY DANDRUFF SHAMPOO TREATMENTNaturich Cosmetique Labs129fd043-6643-cc46-e063-6294a90a6eae2025-10-08WarningsExact identifier
ndc (package): 72496-1038-1
ndc (package): 72496-1038-2
ndc (product): 72496-1038
ndc11 (package): 72496103802
ndc11 (package): 72496103801
spl id: 40abe026-b3d7-cdce-e063-6394a90a0a8b
spl set id: 129fd043-6643-cc46-e063-6294a90a6eae

Reported adverse events (FAERS/openFDA)#

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