DFS 1.5%/MS 25%/MENTH 6%/CAP 0.025% PAK

Nucare Pharmaceuticals Inc🇺🇸 United States

FDA Page

Effective Date: May 4, 2021
Approval ID: 7099d4b1-6893-234a-e053-2991aa0a682b
Products: 1 registered
Version: 2

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

These highlights do not include all the information needed to use Diclofenac Sodium Topical Solution safely and effectively. See full prescribing information for Diclofenac Sodium Topical Solution.DICLOFENAC Sodium Topical Solution 1.5% w/w is for topical use only. Initial U.S. Approval: 1988

Quick Stats

Total Products1

Labelers2

Label Sections33

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.