Drug Facts
Active ingredient
Salicylic Acid (2%)
Shea Moisture
FDA Label NDC 64942-2083
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 64942-2083). 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, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
For best results use at least twice per week or as directed by a doctor. Shake before use. Apply to wet hair, gently massage onto scalp and gently comb for even distribution. Leave on for three minutes, rinse and style as desired.
Inactive Ingredients
Water, Cetearyl Alcohol, Cocos Nucifera (Coconut) Oil, Stearamidopropyl Dimethylamine, Behentrimonium Chloride, Glycerin, Butyrospermum Parkii (Shea) Butter, Acetic Acid, Niacinamide, Gluconolactone, Rosa Damascena Flower Extract, Centella Asiatica (Gotu Kola) Extract, Sodium Benzoate, Fragrance
Questions?
Call us at 1-866-478-1925
* Please review the disclaimer below.
