Mucus Relief Tablet
Product Images NDC 55681-301

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 Mucus Relief (NDC 55681-301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Twin Med 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

Df1 (01b Lbl (df1) Mucus Relief 100cap)

Df1 (01b Lbl (df1) Mucus Relief 100cap)
Drug Facts panel for MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg tablets. Includes active ingredient (Guaifenesin 600 mg) and purpose (expectorant). Lists uses for loosening phlegm, warnings for children under 12 and other precautions, and directions for use including dosing and intake instructions.*
FDA Label Image

Df2 (01b Lbl (df2) Mucus Relief 100cap)

Df2 (01b Lbl (df2) Mucus Relief 100cap)
Drug Facts panel continuation for MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg tablets includes storage information, a list of inactive ingredients, and a toll-free contact number for questions. It also notes that the product is distributed by ProCure Products and clarifies that it is not manufactured or distributed by the trademark owner.*
FDA Label Image

Pdp (01b Lbl (pdp) Mucus Relief 100cap)

Pdp (01b Lbl (pdp) Mucus Relief 100cap)
Label for MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg tablets by PROCURE Healthcare Products. The label states guaifenesin as the active ingredient with extended-release formulation and an expectorant function. The package contains 100 tablets at 600 mg strength, produced by labeler TWIN MED LLC. Additional text references similarity to Mucinex active ingredient.*

* 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.