The packaging material is essential for to avoid the chances of contamination. The selection of packaging materials depends on the fixed medication or pharmaceutical product. Testing involves evaluating glass containers, rubber closures, and plastic materials for chemical resistance, hydrolytic resistance, argon resistance, leakage, transparency, self-sealing ability, fragmentation, and light absorption. Labeling encompasses various dosage forms, including manufacturing and dispensing labels. Prescription bottle labels typically contain instructions for medication use, guided by federal and state laws in the United States that establish legal criteria. Labels serve as displays of textual, printed, or visual content on the packaging or immediate container of medication. The term "labeling" encompasses any written, printed, or visual information on or within the box or wrapper containing a product, excluding external shipping containers. Packaging is a cost-effective method for presenting, protecting, identifying, informing, containing, facilitating use, preserving integrity, and stabilizing a product. Primary, secondary, and tertiary packaging types exist. Containers must uphold a products identity, strength, quality, and purity while preventing contamination. They should meet standards equivalent to those used by manufacturers to package medicinal items and include safety features like child-proof closures.