FDA.reportPublic FDA data

Light Roots

Manufacturer
Raven Innovations LLC
Effective date
2026-09-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-22 03:02:22

Label at a glance#

ProductRestoraScalp Anti Dandruff Dry Light Roots
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

Helps eliminate itching, irritation, and scaling associated with dandruff, seborrheic dermatitis and psoriasis.

Dosage and administration

Shake well before use Hold nozzle close to scalp and spray light layer of powder directly on dry scalp Lightly massage or brush to blend in Apply once daily, 3-5 times a week on non-wash days or as directed by a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff shampoo

Uses

INDICATIONS & USAGE SECTION

Helps eliminate itching, irritation, and scaling associated with dandruff, seborrheic dermatitis and psoriasis.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor

OTC - ASK DOCTOR SECTION

before use if you have a condition that covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

INSTRUCTIONS FOR USE SECTION

Shake well before use
Hold nozzle close to scalp and spray light layer of powder directly on dry scalp
Lightly massage or brush to blend in
Apply once daily, 3-5 times a week on non-wash days or as directed by a doctor

Other information

OTHER SAFETY INFORMATION

Store in a cool dry place at room temperature 15-30°C (59-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Oryza Sativa (Rice) Starch, Maranta Arundinacea Root Powder, Iron Oxides (CI 77499, CI 77491, CI 77492), Kaolin, Allantoin, Chamomilla Recutita (Matricaria) Flower Extract, Vaccinium Macrocarpon (Cranberry) Seed, Triethoxycaprylylsilane, Olea Europaea (Olive) Leaf Extract, Maltodextrin, Camellia Sinensis Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label RestoraScalp Light Roots PF(2)(3)_Page_1RestoraScalp Light Roots PF(2)(3)_Page_1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130202409270231GTIN-13: 0202409270231
EAN-13: 0202409270231
GTIN-12: 202409270231
UPC-A: 202409270231
GTIN storage (14 digits): 00202409270231		RestoraScalp Light Roots PF(2)(3)_Page_1.jpg
BarcodeEAN-130384042000007GTIN-13: 0384042000007
EAN-13: 0384042000007
GTIN-12: 384042000007
UPC-A: 384042000007
GTIN storage (14 digits): 00384042000007		RestoraScalp Light Roots PF(2)(3)_Page_1.jpg
QR code linkQR Codeqrco.de/bePvYqRestoraScalp Light Roots PF(2)(3)_Page_1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84042-10184042-101-01, 84042-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
FERROSOFERRIC OXIDEXM0M87F357IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
KAOLIN24H4NWX5COIACT
FERRIC OXIDE RED1K09F3G675IACT
ALLANTOIN344S277G0ZIACT
MALTODEXTRIN7CVR7L4A2DIACT
STARCH, RICE4DGK8B7I3SIACT
CRANBERRY SEED38ZFO1X2U7IACT
CHAMOMILEFGL3685T2XIACT
MARANTA ARUNDINACEA ROOTFVN346W31AIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
OLEA EUROPAEA LEAFMJ95C3OH47IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-07-10full-release2026-06-01 00:19:35

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
1ce9f1e1-411a-1f32-e063-6294a90a9fe01ce9f1e1-4119-1f32-e063-6294a90a9fe02024-07-10WarningsExact identifier
spl set id: 1ce9f1e1-4119-1f32-e063-6294a90a9fe0

Reported adverse events (FAERS/openFDA)#

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