Mucinex Rapid Clear Day Night And Clear And Cool Nasal Kit
Product Images NDC 72854-213

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mucinex Rapid Clear Day Night And Clear And Cool Nasal (NDC 72854-213). 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 (72854 213 Back Label)

Drug Facts panels for MUCINEX Rapid Clear Day Night and Clear and Cool Nasal Spray kit showing active ingredients and purposes for daytime pain, headache & mucus congestion, nighttime headache, cough & fever, and severe nasal congestion relief. Includes uses, warnings, precautions, and directions for each component.*

FDA Label Image

Carton Label (72854 213 Front Label)

MUCINEX Rapid Clear Day Night and Clear and Cool Nasal cold and sinus value pack kit featuring daytime and nighttime caplets plus a nasal spray. Daytime caplets (12 count) contain acetaminophen and guaifenesin for pain, headache, fever, and mucus congestion relief. Nighttime caplets (8 count) include acetaminophen, dextromethorphan HBr, and triprolidine HCl for headache, cough, fever, and itchy throat relief. The nasal spray (3/4 fl oz) contains oxymetazoline HCl 0.05% for severe nasal congestion, offering fast-acting, 12-hour relief with a cooling menthol flavor. Produced by Reckitt Benckiser LLC.*

FDA Label Image

Full Carton Label (72854 213 Super Back Label)

Drug Facts text panels for MUCINEX Rapid Clear Day Night and Clear and Cool Nasal kit. The panels include warnings about pregnancy and breastfeeding, overdose risks, dosing directions, storage instructions at 20-25°C (68-77°F), active and inactive ingredients, and consumer contact information. Directions specify age restrictions and dosing intervals for daytime and nighttime use. The text emphasizes not exceeding recommended dosages and consulting a doctor for prolonged symptoms or adverse reactions.*

* 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.