Day And Night Severe Sinus Congestion And Cough
Product Images NDC 51013-427

2 FDA label images from Puracap Pharmaceutical Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Day And Night Severe Sinus Congestion And Cough (NDC 51013-427). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puracap Pharmaceutical 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

Carton Back (Cmb66 Back)

Carton Back (Cmb66 Back)
Drug Facts panels for Day and Night Severe Sinus Congestion and Cough Maximum Strength. The panels provide active ingredients, uses, warnings, directions, and other consumer information for both the daytime and nighttime formulations within the product.*
FDA Label Image

Carton Front (Cmb66 Front)

Carton Front (Cmb66 Front)
Day and Night Severe Sinus Congestion and Cough Maximum Strength softgels carton label by PuraCap Pharmaceutical LLC. The label highlights maximum strength relief with separate Day (non-drowsy) and Night formulas, each containing 8-16 liquid filled capsules. The Day formula includes acetaminophen 325 mg, dextromethorphan hydrobromide 10 mg, and phenylephrine hydrochloride 5 mg. The Night formula contains acetaminophen 325 mg, dextromethorphan hydrobromide 10 mg, doxylamine succinate 6.25 mg, and phenylephrine hydrochloride 5 mg. Indications include sinus congestion, sinus pressure, headache, body ache, nasal congestion, runny nose, sneezing, and cough. The label also features a barcode and references comparison to Alka-Seltzer Plus products.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.