Shea Moisture
FDA Label NDC 64942-2085

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Conopco, Inc. D/b/a/ Unilever for the product Shea Moisture (NDC 64942-2085). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active ingredient

Salicylic Acid (1.8%)

Purpose

Anti-dandruff

Uses

Helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

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

Keep this and all drugs out of reach of children.

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

Directions

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.

Inactive Ingredients

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

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