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 23:52:10

Label at a glance#

ProductRE-fresh Scalp Care
Active ingredientSALICYLIC ACID
Label structure10 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 SEA MINERAL + HYDRATE ANTI-DANDRUFF CONDITIONER - salicylic acid liquid

DESCRIPTION SECTION

RE-fresh Scalp Care Sea Mineral + Hydrate Anti-Dandruff Conditioner

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 and flaking associated with dandruff.

Warning

WARNINGS SECTION

• For external use only
• When using this product: Avoid contact with eyes. If contact occurs, rinse eyes thoroughtly 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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cetearyl Alcohol, Stearamidopropyl Dimethylamine, Behentrimonium Chloride, Cocos Nucifera (Coconut) Oil, Sea Salt, 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, Propylene Glycol, Fragrance (Parfum), Sodium Benzoate, Dipropylene Glycol, Disodium EDTA, Benzyl Alcohol, Benzyl Benzoate, Benzyl Salicylate.

Questions/comments?

OTC - QUESTIONS SECTION

Call toll-free 1-800-671-3998

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RefreshMineralSeaCDRefreshMineralSeaCD

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
64942-1637-12023-07-28C16284748780-1ba0f9c33-3b0d-a910-e053-dadaa90a0b85RE-fresh Scalp Care Sea Mineral + Hydrate Anti-Dandruff Conditioner
64942-1637-12021-12-01C16284748780-1ba0f9c33-3b0d-a910-e053-dadaa90a0b85RE-fresh Scalp Care Sea Mineral + Hydrate Anti-Dandruff Conditioner
64942-1637-12021-01-29C16284748780-1ba0f9c33-3b0d-a910-e053-dadaa90a0b85RE-fresh Scalp Care Sea Mineral + Hydrate Anti-Dandruff Conditioner

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1637-1RE-fresh Scalp Care400 mL in 1 CONTAINERLIQUID4003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1637RE-FRESH SCALP CARE (SALICYLIC ACID) LIQUID [CONOPCO, INC. D/B/A/ UNILEVER]3Legacy NDC, 1 package rows20221208_84601226-87d2-2d4e-e053-2a91aa0afc35.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-163764942-1637-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARAMIDOPROPYL DIMETHYLAMINEK7VEI00UFRIACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
COCONUT OILQ9L0O73W7LIACT
SEA SALT87GE52P74GIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
GINKGO19FUJ2C58TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
DIPROPYLENE GLYCOLE107L85C40IACT
BENZYL ALCOHOLLKG8494WBHIACT
BENZYL BENZOATEN863NB338GIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
SALICYLIC ACIDO414PZ4LPZACTIB
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT

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-9d68-b242-e053-2a95a90ac87684601226-87d2-2d4e-e053-2a91aa0afc352022-12-07WarningsExact identifier
spl id: ef3f84ad-9d68-b242-e053-2a95a90ac876
spl set id: 84601226-87d2-2d4e-e053-2a91aa0afc35

Reported adverse events (FAERS/openFDA)#

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