St. Ives Lotion
FDA Label NDC 64942-1861

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 St. Ives (NDC 64942-1861). 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 active ingredient, 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.

Inactive Ingredients

Water (Aqua), Cellulose, Caprylic/Capric Triglyceride, Steareth-2, Glycerin, Magnesium Aluminum Silicate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Steareth-21, Phenoxyethanol, Jojoba Esters, Menthol, Xanthan Gum, Helianthus Annuus (Sunflower) Seed Wax, Sodium Phytate, Niacinamide, Polyglycerin-3, Acacia Decurrens Flower Wax, Tasmannia Lanceolata Fruit/Leaf Extract, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract.

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