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  5. Label Information: Docusate Sodium 250mg

FDA Label for Docusate Sodium 250mg

View Indications, Usage & Precautions

Table of Contents

    1. OTC - ACTIVE INGREDIENT
    2. OTC - PURPOSE
    3. OTC - KEEP OUT OF REACH OF CHILDREN
    4. INDICATIONS & USAGE
    5. DOSAGE & ADMINISTRATION
    6. WARNINGS
    7. INACTIVE INGREDIENT
    8. PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Docusate Sodium 250mg Product Label

The following document was submitted to the FDA by the labeler of this product Olds Softgels 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.

Otc - Active Ingredient



ACTIVE INGREDIENT

Docusate Sodium 250 mg


Otc - Purpose



IMPORTANT

This is a bulk shipment, intended for further processing only. It is not to be used in its present condition and it should be repackaged immediately and labeled strictly in conformance with the Federal Food, Drug and Cosmetic Act and other pertinent government regulations. 


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.


Indications & Usage



Olds SoftGels Inc


Dosage & Administration



All complaints or claims for allowances of any kind must be made within 10 days after receipt of goods.


Warnings



All complaints or claims for allowances of any kind must be made within 10 days after receipt of goods.


Inactive Ingredient



INACTIVE INGREDIENTS

Red No. 40

Granular FD and C

Yellow No.6

Granular

Gelatin

Glycerin USP 99 Percent

Polyethylene

Glycol 400 USP PEG 400

Propylene glycol

Purified water

Sorbitol special GC


* Please review the disclaimer below.