Oral Saline Laxative
Product Images NDC 0363-0126

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Oral Saline Laxative (NDC 0363-0126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Co, 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

Walgreens Oral Saline Drug Facts 2 (086fba92 75d0 4c2b Abcd 72ba10b86574 00)

Drug Facts panel for Oral Saline Laxative by Walgreen Co. This section includes other information about the product's active ingredient content (sodium 556 mg per teaspoon), storage instructions, inactive ingredients such as cherry flavor and glycerin, and a tamper-evident safety warning about the bottle seal. It also lists a customer service phone number.*

FDA Label Image

Walgreens Oral Saline Drug Facts 1 (086fba92 75d0 4c2b Abcd 72ba10b86574 01)

Drug Facts text panels for Oral Saline Laxative by Walgreen Co detail active ingredients dibasic sodium phosphate 0.9g and monobasic sodium phosphate 2.4g per teaspoon, intended as a saline laxative. The panels provide usage instructions for occasional constipation, dosage limits by age, important warnings regarding medical conditions, potential side effects, and precautions including consulting a doctor before use and avoiding overdose.*

FDA Label Image

Walgreens Phosphate Oral Saline Laxative Principal Display Panel (086fba92 75d0 4c2b Abcd 72ba10b86574 02)

Label for Oral Saline Laxative Phosphate, sugar free single dose, cherry flavor, 1.5 fl oz (45 mL). The product is distributed by Walgreens Co and is marked with 100% satisfaction guaranteed. The label has Walgreens branding and indicates the product is for relief of occasional constipation.*

* 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.