Humco Dewees Carminative Suspension
Product Images NDC 0395-0713

3 FDA label images from Humco Holding Group, Inc. · 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 Humco Dewees Carminative (NDC 0395-0713). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Humco Holding Group, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

New (Doc120717)

New (Doc120717)
Drug Facts panel for Humco Dewees Carminative suspension with active ingredient magnesium carbonate 250 mg per 5 mL as antacid. Includes indications for upset or sour stomach, warnings about kidney disease and dosage limits, directions for use by age group, inactive ingredients list, and packaging and safety seal information.*
FDA Label Image

Dewees

Dewees
Drug Facts panel for Humco Dewees Carminative Antacid suspension, 50 mg/mL magnesium carbonate. Includes active ingredient purpose, indications, warnings, directions for use, and a list of inactive ingredients. It also provides safety warnings about tamper-evident seals and manufacturer contact information for Humco Holding Group, Inc.*
FDA Label Image

Old (Old Label)

Old (Old Label)
Drug Facts label for Humco Dewees Carminative suspension, containing magnesium carbonate 250 mg per 5 mL as the active ingredient. The label includes warnings, usage directions for adults and children, inactive ingredients, and safety sealing information. It specifies dosing instructions and cautions on use during pregnancy, breastfeeding, and kidney disease.*

* 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.