V Relief Serum Gel
FDA Label NDC 84528-682

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kindra for the product V Relief Serum (NDC 84528-682). 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, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Use

→ Warnings

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Questions?

→ Principal Display Panal

Active Ingredient

Dimethicone 2%

Purpose

Skin Protectant

Use

helps prevent, temporarily protects, and helps relieve chafed, chapped, or cracked skin

Warnings

For external use only

Otc - When Using

When using this product do not get into eyes

Otc - Stop Use

Stop use and ask a doctor if

condition worsens
symptoms last more than 7 days or clear up and occur again within a few days

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

apply generously as needed

Inactive Ingredients

Water, Hydroxypropyl Starch Phosphate, Propanediol, Glycerin, Butyrospermum Parkii (Shea) Butter, Lactic Acid, Sodium Benzoate, Potassium Sorbate, Hydrogenated Lecithin, Akebia Quinata Extract, Sodium Hyaluronate, Phenethyl Alcohol, Ethylhexylglycerin, Maltodextrin, Pentapeptide-59, Tocopheryl Acetate (Vitamin E), Cocos Nucifera (Coconut) Oil