Anti Dandruff

Manufacturer
Profectus Beauty, LLC
Effective date
2022-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:51:24

Label at a glance#

ProductAnti Dandruff
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis

Dosage and administration

█ For best results use at least twice a week or as directed by a doctor. █ For maximum dandruff control, use every time you shampoo. █ Shake before use, wet hair, massage onto scalp, leave on scalp for several minutes, rinse, repeat if desired.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 3.0%

Uses

INDICATIONS & USAGE SECTION

Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis

Purpose

OTC - PURPOSE SECTION

Anti-Dandruff, Anti-Seborrheic Dermatitis, Anti-Psoriasis

Warnings

WARNINGS SECTION

Because we utilize as many naturally derived ingredients as
possible, our products may vary in color over time and with each new batch
we make. These natural variations do not in any way affect the quality of
efficacy of the product.
█ For external use only. █ Ask a doctor before use if you have a condition
that covers a large area of the body █ Avoid contact with eyes. If contact
occurs, rinse eyes thoroughly with water. █ Stop use and ask a doctor if the
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 the reach of children. If swallowed, get medical help
or contact the Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

█ For best results use at least twice a week or as directed by a doctor.
█ For maximum dandruff control, use every time you shampoo.
█ Shake before use, wet hair, massage onto scalp, leave on scalp for
several minutes, rinse, repeat if desired.

Other Information

OTHER SAFETY INFORMATION

Store in a cool, dry place

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Coco-Sulfate,
Cocamidopropyl Betaine, Glycerin, Aloe Barbadensis Leaf Juice, Fragrance,
Decyl Glucoside, Camellia Sinensis Leaf Extract, Hydrolyzed Quinoa,
Simmondsia Chinensis (Jojoba) Seed Oil, Prunus Amygdalus Dulcis (Sweet
Almond) Oil, Xylitol, Hydrolyzed Soy Protein, Triethyl Citrate, Gluconolactone,
Polyquaternium-7, Phenoxyethanol, Benzyl Alcohol, Sodium Benzoate,
Potassium Sorbate.

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll free 1-888-237-4131 or visit www.keranique.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70550-32970550-329

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205023salicylic acid 3 % Medicated ShampooPSN2
205023salicylic acid 30 MG/ML Medicated ShampooSCD2
205023salicylic acid 3 % Medicated ShampooSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70550-329-012024-01-30C16284748780-11030e365-12cb-111a-e063-dadaa90a10e2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70550-329-01Anti Dandruff1 in 1 CARTONLOTION12
70550-329-01Anti Dandruff240 mL in 1 BOTTLE, PLASTICLOTION2402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70550-329ANTI DANDRUFF (KERANIQUE ANTI DANDRUFF SHAMPOO) LOTION [PROFECTUS BEAUTY, LLC]2Legacy NDC, 2 package rows20221107_6ce5f0d0-efbb-4a6a-a813-544586b16f72.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70550-32970550-329-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
ecd389e1-213e-24bc-e053-2a95a90ad5566ce5f0d0-efbb-4a6a-a813-544586b16f722022-11-06WarningsExact identifier
spl id: ecd389e1-213e-24bc-e053-2a95a90ad556
spl set id: 6ce5f0d0-efbb-4a6a-a813-544586b16f72

Reported adverse events (FAERS/openFDA)#

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