Redicare Nasal And Sinus Decongestant Tablet
Product Images NDC 71105-272

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 Redicare Nasal And Sinus Decongestant (NDC 71105-272). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redicare 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

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2f24e451 785b 4395 E063 6394a90ad458
Redicare Nasal and Sinus Decongestant 10 mg oral tablet, round and dark red, embossed with the number '272'. Labeler is Redicare LLC. This image shows a single tablet intended for nasal and sinus decongestion.*
FDA Label Image

Packet (Decongestant 02 Packet)

Packet (Decongestant 02   Packet)
Label for Redicare Nasal and Sinus Decongestant tablets, each containing phenylephrine HCl 10 mg. The package includes 2 tablets and is manufactured by Redicare LLC. The label presents directions for use, warnings, storage instructions, and states it is not for individual sale.*
FDA Label Image

Principal Image (Decongestant 107x86x63 08feb2025 03)

Principal Image (Decongestant 107x86x63 08feb2025 03)
Packaging label for Redicare Nasal and Sinus Decongestant 10 mg oral tablets by Redicare LLC. The label indicates the product contains 100 tablets and is labeled as a decongestant comparable to ingredients in Sudafed Congestion. The design features orange and white colors with the Redicare logo, barcode, and drug facts panels including active ingredient, uses, warnings, directions, other information, and inactive ingredients. The label also shows contact information for Redicare LLC and states the product is made in the USA.*

* 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.