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  5. Label Information: Entsol

FDA Label for Entsol

View Indications, Usage & Precautions

Table of Contents

    1. ACTIVE INGREDIENT:
    2. PURPOSE:
    3. INACTIVE INGREDIENTS
    4. PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CONTAINER
    5. PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CARTON

Entsol Product Label

The following document was submitted to the FDA by the labeler of this product Pharmaderm, A Division Of Fougera Pharmaceuticals Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredient:



Sodium chloride (3%)


Purpose:



Moisturizer


Inactive Ingredients



Purified Water, Sodium Phosphate - Dibasic, Potassium Phosphate - Monobasic.


Package Label – Principal Display Panel – Container



NDC 10337-311-10

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – LABEL - entsol 01

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – LABEL - entsol 01


Package Label – Principal Display Panel – Carton



NDC 10337-311-10

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CARTON - entsol 02

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CARTON - entsol 02


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