Zephrex D Capsule, Gelatin Coated
Product Images NDC 0113-0401

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Zephrex D (NDC 0113-0401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by L. Perrigo Company, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Zephrex-d Image (04 18 17 1w962pec1 Only Image.png)

Zephrex-d Image (04 18 17 1w962pec1 Only Image.png)
ZEPHREX-D is a nasal decongestant that temporarily relieves nasal and sinus congestion and pressure caused by the common cold, hay fever, or other upper respiratory allergies. The active ingredient in each softgel is not specified. The drug should not be used if you are taking prescription monoamine oxidase inhibitor drugs for depression, psychiatric, emotional conditions or Parkinson’s disease, or for 2 weeks after stopping the medication. Before taking this product, ask a doctor or pharmacist if you are taking prescription drugs that contain monoamine oxidase inhibitors. People with certain medical conditions, such as heart disease, high blood pressure, thyroid disease, diabetes or difficulty urinating due to an enlarged prostate gland, should ask a doctor before use. If the symptoms do not improve within 7 days or occur with fever, stop use and seek medical attention. Children under 6 years should not use this product. Dosage instructions are provided for adults and children aged 6 to 12 years. The product does not specify the active ingredient. The product contains inactive ingredients such as polysorbate 80, polyethylene glycol, and aluminum. ZEPHREX-D is distributed by Perrigo.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.