Arthritis Hand
FDA Label NDC 59779-507

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cvs for the product Arthritis Hand (NDC 59779-507). 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, when using this product, stop using this product and ask a doctor if, 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

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

for washing to decrease bacteria on the skin.

Warnings

For external use only.

When Using This Product

  • avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop Using This Product And Ask A Doctor If

  • irritation and redness develops.

Keep Out Of Reach Of Children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Squeeze a small amount onto a wet wash cloth, sponge, pouf or hands and apply to body. Work into a rich lather and rinse off.

Questions Or Comments?

1-800-746-7287

Inactive Ingredients

Water (Aqua), Cocamidopropyl Betaine, Decyl Glucoside, Hydroxyethylcellulose, Glycerin, Citric Acid, Poloxamer 124, Fragrance (Parfum), Tetrasodium EDTA, Polyquaternium-7, Sodium Citrate, Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).

Label Copy

Image Of The Label (20874l)

Image Of The Label (20874l)

* Please review the disclaimer below.