Drugplain

Dynarex Povidone Iodine Prep Solution 10 mg/mL

Povidone Iodine Prep Solution · LIQUID · Dynarex Corporation

No Recall History
Plain English

Dynarex Povidone Iodine Prep Solution is a liquid containing povidone iodine prep solution at 10 mg/mL, taken topical. Manufactured by Dynarex Corporation.

Key Facts

Brand Name
Dynarex Povidone Iodine Prep Solution
Generic Name
Povidone Iodine Prep Solution
NDC Code (Product)
67777-141
Manufacturer
Dynarex Corporation
Strength
10 mg/mL
Dosage Form
LIQUID
Route
TOPICAL
Marketing Status
Application #
M003
Drug Class
Antiseptic [EPC]
Marketing Start
05/08/2018

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Use For preparation of the skin prior to surgery. Helps reduce bacteria that potentially can cause skin infection

Dosage & Administration

Directions Clean the area. Apply product to the operative site prior to surgery.

Warnings

Warnings For external use only Do Not Use if allergic to iodine in the eyes Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is Dynarex Povidone Iodine Prep Solution used for?

Dynarex Povidone Iodine Prep Solution contains Povidone Iodine Prep Solution. It is a liquid taken topical. Consult your doctor for specific uses.

Is Dynarex Povidone Iodine Prep Solution a controlled substance?

Dynarex Povidone Iodine Prep Solution is not classified as a controlled substance by the DEA.

What is the generic name for Dynarex Povidone Iodine Prep Solution?

The generic name for Dynarex Povidone Iodine Prep Solution is Povidone Iodine Prep Solution. There are 1 other brand versions of Povidone Iodine Prep Solution.

What is the NDC code for Dynarex Povidone Iodine Prep Solution 10 mg/mL?

The NDC (National Drug Code) for Dynarex Povidone Iodine Prep Solution 10 mg/mL is 67777-141, listed by Dynarex Corporation.

Product NDC

67777-141

Package NDC

67777-141-31

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)