Coltalin Tablet
Product Images NDC 51467-011

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 Coltalin (NDC 51467-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fortune Pharmacal Company Limited, 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

Image Of Carton (Coltalin Unit Box 24s Reduced Size)

Image Of Carton (Coltalin Unit Box 24s Reduced Size)
COLTALIN cold, flu, and hay fever relief oral tablets packaging label. The label lists active ingredients acetaminophen, chlorpheniramine maleate, and phenylephrine hydrochloride. Contains 24 tablets per package and is distributed by Fortune Pharmacal Company Limited. The carton includes bilingual English and Chinese text describing multi-symptom relief properties and usage warnings. The packaging is predominantly white with green and blue accents, including the brand name COLTALIN prominently displayed.*
FDA Label Image

Image Of Carton (Coltalin Unit Box 36s Reduced Size)

Image Of Carton (Coltalin Unit Box 36s  Reduced Size)
Packaging label for COLTALIN oral tablets containing Acetaminophen, Chlorpheniramine maleate, and Phenylephrine hydrochloride. The label highlights its use for cold, flu, and hay fever multi-symptom relief. The package contains 36 tablets and is manufactured by Fortune Pharmacal Company Limited. The label includes bilingual text in English and Chinese, safety seal indication, and dosage information.*

* 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.