Nystatin Suspension
Product Images NDC 0121-0868

3 FDA label images from Pai Holdings, Llc Dba Pai Pharma · 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 Nystatin (NDC 0121-0868). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

5 mL Unit Dose Cup Label (5 mL Cup Label)

5 mL Unit Dose Cup Label (5 mL Cup Label)
Nystatin Oral Suspension, USP 500,000 units per 5 mL vial label by Pharmaceutical Associates, Inc. It delivers 5 mL and contains alcohol ≤ 1% v/v. The label includes the NDC 0121-0868-05 and states 'Rx Only' for institutional use, with instructions to shake well and see the insert for details.*
FDA Label Image

60 mL Bottle Label (60 mL Bottle Label)

60 mL Bottle Label (60 mL Bottle Label)
Label of Nystatin Oral Suspension, USP 100,000 units per mL, a cherry peppermint flavored suspension for oral use. The 60 mL bottle label from PAI Holdings, LLC dba PAI Pharma includes directions to shake well, contains a calibrated dropper, and cautions about tamper evidence. The label also provides storage instructions and warnings, including keeping out of reach of children and avoiding freezing.*
FDA Label Image

Nystatin Chemical Structure (Nystatin Chemical Structure)

Nystatin Chemical Structure (Nystatin Chemical Structure)
Chemical structure diagram of the active ingredient nystatin, showing its complex polyene macrolide arrangement with multiple hydroxyl groups and double bonds.*

* 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.