Mucinex Insta Soothe Spray
Product Images NDC 72854-266

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mucinex Insta Soothe (NDC 72854-266). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reckitt Benckiser Llc, 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

Back Label (Mucinex Insta Label)

Back Label (Mucinex Insta Label)
This is a Drug Facts label for a product that contains the active ingredients Benzocaine 5% and Menthol 2% as oral pain relievers to temporarily relieve minor irritation and pain associated with sore throat, sore mouth, and canker sores. The label includes warnings of potential risks associated with using the product, including the risk of methemoglobinemia, a potential allergic reaction to local anesthetics, and the need to consult a doctor if symptoms persist. The label also cautions against using the product for teething in children under five years of age and advises users not to exceed the recommended dosage.*
FDA Label Image

Front Label (Mucinex Instasoothe Label Front)

Front Label (Mucinex Instasoothe Label Front)
This is a description of a throat spray product called "Kickstart" by Mucinex. It is alcohol-free and contains benzocaine and menthol as oral pain relievers. The spray has a winterfresh flavor and comes in a 6l bottle. The label includes a product code (NDT 72854-268-04) and a number (030723 3257157) which may refer to manufacturing or batch information.*
FDA Label Image

Back Label (Mucinex Instasoothe Back Label)

Back Label (Mucinex Instasoothe Back Label)
This is a drug information label indicating usage instructions, precautions, and inactive ingredients for a medication that may help to soothe a sore mouth. Users are advised to stop using the drug if sore mouth symptoms do not improve within a few days. The drug should not be used if pregnant or breastfeeding unless advised by a doctor. Instructions dictate that adults and children over 12-years old should apply the drug to the affected area up to four times per day, while younger children should only use the drug under adult supervision. The listed inactive ingredients include citric acid, cetylpyridinium chloride, and others. For questions or to report side effects, call 1-866-MUCINEX.*

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