Loperamide Hydrochloride Solution
Product Images NDC 17856-6836

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Loperamide Hydrochloride (NDC 17856-6836). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Label1 (17856 6836 01)

Label for loperamide hydrochloride oral solution, strength 1 mg/7.5 mL, supplied in a package containing 72 cups. The label displays dosage, storage instructions to keep between 20°-25°C (68°-77°F), and warnings to keep out of reach of children. It lists Atlantic Biologicals Corp. as the distributor and includes a barcode and reorder phone number.*

FDA Label Image

Label2 (17856 6836 02)

Label for loperamide hydrochloride oral solution with a strength of 2 mg/15 mL. The label states the package delivers 15 mL per dose and includes storage instructions to keep between 20°-25°C (68°-77°F) and to keep out of reach of children. The product is labeled as an OTC drug with a quantity of 50 cups, packaged by Unit Dose Solutions and distributed by Atlantic Biologicals Corp.*

FDA Label Image

Label3 (17856 6836cup)

Two labels for loperamide HCl oral suspension. The left label is for a 2 mg/15 mL strength, delivering 15 mL per dose, and the right label is for a 1 mg/7.5 mL strength, delivering 7.5 mL per dose. Both labels state the product is an anti-diarrheal distributed by Atlantic Biologicals Corp., Morrisville, NC.*

* 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.