FDA.reportPublic FDA data

Shea Moisture

Manufacturer
Conopco, Inc. d/b/a/ Unilever
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:36:22

Label at a glance#

ProductShea Moisture
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

Helps prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

Apply to affected areas one to four times daily or as directed by a doctor. Shake before use. Apply directly onto wet or dry scalp. Gently squeeze bottle while moving tip from front to back of your scalp. Repeat until entire scalp is covered. Massage for even distribution. Do not rinse.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic Acid (1.8%)

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

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

Apply to affected areas one to four times daily or as directed by a doctor. Shake before use. Apply directly onto wet or dry scalp. Gently squeeze bottle while moving tip from front to back of your scalp. Repeat until entire scalp is covered. Massage for even distribution. Do not rinse.

Other information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Niacinamide, Butyrospermum Parkii (Shea) Butter, Acetic Acid, PEG-40 Hydrogenated Castor Oil, Gluconolactone, Rosmarinus Officinalis (Rosemary) Extract, Centella Asiatica (Gotu Kola) Extract, Hydroxyethylcellulose, Sodium Hydroxide, Menthol, Citric Acid, Sodium Benzoate, Fragrance

Questions?

OTC - QUESTIONS SECTION

Call us at 1-866-478-1925

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Shea Butter Apple Cider Anti-dandruff Leave-InShea Butter Apple Cider Anti-dandruff Leave-In

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2050067salicylic acid 1.8 % Topical OilPSN2
2050067salicylic acid 18 MG/ML Topical OilSCD2
2050067salicylic acid 1.8 % Topical OilSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2085-1Shea Moisture118 mL in 1 BOTTLELIQUID1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2085SHEA MOISTURE (APPLE CIDER VINEGAR ANTI-DANDRUFF LEAVE-IN) LIQUID [CONOPCO, INC. D/B/A/ UNILEVER]2Legacy NDC, 1 package rows20241109_e5e7ca6d-8d37-626b-e053-2a95a90ab91b.zip

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
64942-208564942-2085-1

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
SODIUM BENZOATEOJ245FE5EUIACT
MENTHOLL7T10EIP3AIACT
SHEA BUTTERK49155WL9YIACT
WATER059QF0KO0RIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
SODIUM HYDROXIDE55X04QC32IIACT
ACETIC ACIDQ40Q9N063PIACT
GLYCERINPDC6A3C0OXIACT
NIACINAMIDE25X51I8RD4IACT
SALICYLIC ACIDO414PZ4LPZACTIB
GLUCONOLACTONEWQ29KQ9POTIACT
ROSEMARYIJ67X351P9IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
26521992-2558-c88b-e063-6394a90a8c40e5e7ca6d-8d37-626b-e053-2a95a90ab91b2024-11-07WarningsExact identifier
spl id: 26521992-2558-c88b-e063-6394a90a8c40
spl set id: e5e7ca6d-8d37-626b-e053-2a95a90ab91b

Reported adverse events (FAERS/openFDA)#

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