Kirkland Signature Lansoprazole Capsule, Delayed Release
Product Images NDC 63981-582

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 Kirkland Signature Lansoprazole (NDC 63981-582). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Costco Wholesale Company, 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

Lansoprazole Package Image 1 (Image 01)

Lansoprazole Package Image 1 (Image 01)
This is a description for a medication product that is used in treating frequent heartburn. The product is similar to PREVACID 24HR; the active ingredient is not specified. The treatment may take between 1 to 4 days to attain full effect. The medication is sodium-free and each package contains three courses of treatment, each lasting for 14 days. The product is manufactured by Kirkland. The NDC code and product number are 63981-582-03 and 805287, respectively.*
FDA Label Image

Lansoprazole Package Image 2 (Image 02)

Lansoprazole Package Image 2 (Image 02)
This is a drug label that likely comes with a package of acid reducing capsules that can be used for 14-day courses to treat heartburn in individuals aged 18 years and older. The medicine should not be used for over 14 days or more often than every 4 months unless directed by a doctor. It is essential to read and follow the instructions, warnings, and package insert before using the product. Some factors require the user to contact a doctor or pharmacist before using the medicine, such as if the person is taking prescription drugs or is pregnant.*

* 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.