Equaline
Product Images NDC 41163-728

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Equaline (NDC 41163-728). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Supervalu Inc., 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

Equaline Nasal Spray (Equaline Nasal Spray)

Equaline Nasal Spray (Equaline Nasal Spray)
EQUALINE® Fast Acting Nasal Spray contains 1% of Phenylephrine hydrochloride as the active ingredient, which acts as a nasal decongestant. It is used to provide temporary relief of nasal congestion due to hay fever, the common cold, or upper respiratory allergies. This product should not be used if its printed seal over the cap is torn or missing. It should not be used for more than three days or exceed the recommended dosage. The container should not be shared between more than one person to avoid the spread of infection. In case of recurrent or worsening congestion, sinus pressure, swollen nasal membranes, or symptoms that persist, the use of the product should be discontinued, and a doctor should be consulted. Adults and children over 12 years old can use 2-3 sprays in each nostril every 4 hours. The product should be stored between 20°-25°C (68°F-77°F) and kept out of reach of children. The inactive ingredients of the nasal spray are benzalkonium chloride, benzyl alcohol, citric acid, purified water, and sodium citrate.*

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