Vanacof Liquid
Product Images NDC 58809-999

View Photos of 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 Vanacof (NDC 58809-999). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gm Pharmaceuticals, 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.

FDA Label Image

Principal Display Panelndc 58809-999-01vanacof®each 5 mL (1 Teaspoonful) Contains:chlophedianol Hydrochloride ….. 12.5 mgdexchlorpheniramine Maleate ….. 1 mgpseudoephedrine Hydrochloride ….. 30mg (Vanacof 01)

Principal Display Panelndc 58809-999-01vanacof®each 5 mL (1 Teaspoonful) Contains:chlophedianol Hydrochloride	….. 12.5 mgdexchlorpheniramine Maleate	….. 1 mgpseudoephedrine Hydrochloride 	….. 30mg (Vanacof 01)
This is a bottle of VANACOF* that should be kept in a tight container with a child-resistant cap. The bottle contains sugar-free, alcohol-free, and dye-free liquid with Tutti Frutti flavor. Each teaspoonful (5 mL) contains Chiophedanol Hydrochloride (12.5 mg), Dexchiorpheniramine Maeate (1 mg), and Pseudosphedrine Hydrochloride (30 mg) for cough relief, antihistamine, and decongestant effects. The product is distributed by GM Pharmaceuticals in Texas and should not be dispensed to consumers. The bottle seal must not be broken or missing. US Patent #9,050,289 and NDC 58809-999-01 are listed.*
FDA Label Image

Principal Display Panelndc 58809-999-01vanacof®each 5 mL (1 Teaspoonful) Contains:chlophedianol Hydrochloride ….. 12.5 mgdexchlorpheniramine Maleate ….. 1 mgpseudoephedrine Hydrochloride ….. 30mg (Vanacof 02)

* 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.