Gumsol Spray
Product Images NDC 52083-714

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 Gumsol (NDC 52083-714). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Gum714nw

Gum714nw
This is a drug product with the NDC code 52083-714-01 that relieves toothaches and minor mouth sores or injuries. It may also be used for denture or orthodontic pain. However, it has warnings for methemoglobinemia which reduces the oxygen carried in the blood, causing pale blue-colored skin, headache, rapid heart rate, shortness of breath, and fatigue. It also has an allergy alert for people with a history of allergic reactions to certain anesthesia. The drug should not be used for more than seven days, more than directed, and in children under two years old. Pregnant or breast-feeding women should consult with healthcare professionals before using the drug. If the sore in the mouth does not improve in seven days, users must stop using it and seek medical attention. Besides, the drug contains phenylketonurics that are harmful to people with a certain condition. The drug should be stored at a controlled room temperature or 15°C-30°C (55F-86°F). The inactive ingredients in the drug are aspartame, cetylpyridinium chloride, menthol, methylparaben, peppermint flavor, propylene glycol, propylparaben, and water (purified). It is manufactured in the USA for Kramer Novis, San Juan, PR 00917.*

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