FDA.reportPublic FDA data

RE-fresh Scalp Care

Manufacturer
Conopco, Inc. d/b/a/ Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:09

Label at a glance#

ProductRE-fresh Scalp Care
Active ingredientSALICYLIC ACID
Label structure11 sections

Dosage and administration

For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

Label contents#

Full prescribing information#

RE-FRESH SCALP CARE EUCALYPTUS + COOLING RELIEF ANTI-DANDRUFF SHAMPOO - salicylic acid liquid

DESCRIPTION SECTION

RE-fresh Scalp Care Eucalyptus + Cooling Relief Anti-Dandruff Shampoo

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic Acid (2.0%)

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if: Condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

Other Information

OTHER SAFETY INFORMATION

Product contains menthol. If you experience discomfort, please stop using.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Salix Alba (Willow) Bark Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Arctium Lappa Root Extract, Ginkgo Biloba Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Hippophae Rhamnoides Fruit Extract, Eucalyptus Globulus Leaf Oil, Citric Acid, Fragrance (Parfum), Sodium Benzoate, Glycerin, Menthol, Polyquaternium-10, Disodium EDTA, Benzyl Salicylate. Citral, Hexyl Cinnamal, Limonene, Linalool.

Questions, comments?

OTC - QUESTIONS SECTION

Call 1-800-761-3683

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RFSCEucalyptusSDRFSCEucalyptusSD

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205104salicylic acid 2 % Medicated ShampooPSN3
205104salicylic acid 20 MG/ML Medicated ShampooSCD3
205104salicylic acid 2 % Medicated ConditionerSY3
205104salicylic acid 2 % Medicated ShampooSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1635-12023-07-28C16284748780-1ba0f9c33-4f1c-a910-e053-dadaa90a0b85RE-fresh Scalp Care Eucalyptus + Cooling Relief Anti-Dandruff Shampoo
64942-1635-12021-12-01C16284748780-1ba0f9c33-4f1c-a910-e053-dadaa90a0b85RE-fresh Scalp Care Eucalyptus + Cooling Relief Anti-Dandruff Shampoo
64942-1635-12021-01-29C16284748780-1ba0f9c33-4f1c-a910-e053-dadaa90a0b85RE-fresh Scalp Care Eucalyptus + Cooling Relief Anti-Dandruff Shampoo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1635-1RE-fresh Scalp Care400 mL in 1 CONTAINERSHAMPOO4003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1635RE-FRESH SCALP CARE (SALICYLIC ACID) SHAMPOO [CONOPCO, INC. D/B/A/ UNILEVER]3Legacy NDC, 1 package rows20221208_84254350-e375-be47-e053-2991aa0ac340.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-163564942-1635-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM CHLORIDE451W47IQ8XIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
GINKGO19FUJ2C58TIACT
EUCALYPTUS OIL2R04ONI662IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM BENZOATEOJ245FE5EUIACT
GLYCERINPDC6A3C0OXIACT
MENTHOLL7T10EIP3AIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
CITRALT7EU0O9VPPIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
ef3f84ad-9d67-b242-e053-2a95a90ac87684254350-e375-be47-e053-2991aa0ac3402022-12-07WarningsExact identifier
spl id: ef3f84ad-9d67-b242-e053-2a95a90ac876
spl set id: 84254350-e375-be47-e053-2991aa0ac340

Reported adverse events (FAERS/openFDA)#

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