Spa Dry Heel Foot Relief Cream
FDA Label NDC 68828-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Distribuidora Comercial Jafra, S.a. De C.v. for the product Spa Dry Heel Foot Relief (NDC 68828-002). 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, warning, direction, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Dimethicone 4%

Purpose

Skin protectant

Uses

  • Helps prevent and temporarily protects chapped or cracked skin

Warning

For external use only
When using this product ● do not get into eyes
Stop use and ask a doctor ● condition worsens ● symptoms last more than 7 days or clear up and occur again in a few days
Do not use on ● deep or puncture wounds ● animal bites ● serious burns
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Direction


• apply as needed

Inactive Ingredients

Water, Caprylic/Capric Triglyceride, Glycerin, Polyisobutene, Butyrospermum Parkii (Shea) Butter, Stearyl Stearate, Isopropyl Palmitate, Cetearyl Alcohol, Cetyl Alcohol, Di-PPG-3 Myristyl Ether Adipate, Myristyl Myristate, Ceteareth-20, Behenyl Alcohol, Niacinamide, Sodium PCA, Lactic Acid, Olea Europaea (Olive) Fruit Oil, Fragrance, Phenoxyethanol, Xanthan Gum, Caprylyl Glycol, Allantoin, Persea Gratissima (Avocado) Oil, Tocopheryl Acetate, Phytosterols, Ethylhexylglycerin, Hexylene Glycol, Panthenol, Disodium EDTA

Product Label

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