Uroav-b
Product Images NDC 15338-503

3 FDA label images from Apace Packaging, Llc · 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 Uroav-b (NDC 15338-503). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apace Packaging, Llc, 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

6cbe6895 5161 8df3 E053 2991aa0a6bcd

6cbe6895 5161 8df3 E053 2991aa0a6bcd
UroAv-B Urinary Antiseptic label showing active ingredients per capsule including Methenamine 118 mg and Sodium Phosphate Monobasic 40.8 mg. The label states the product contains 100 capsules, is Rx only, and provides dosage instructions for adults and pediatric use. The labeler is AVKARE with NDC 42291-852-01.*
FDA Label Image

Label 1 (Screen Shot 2016 03 25 At 3.19.13 Pm)

Label 1 (Screen Shot 2016 03 25 At 3.19.13 Pm)
UroAv-B Urinary Antiseptic capsule label showing active ingredients methenamine 118 mg, sodium phosphate monobasic 40.8 mg, phenyl salicylate 36 mg, methylene blue 10 mg, and hyoscyamine sulfate 0.12 mg per capsule. The label indicates a quantity of 100 capsules and states 'Rx Only'. Dosage instructions for adults and pediatric patients, and a patient advisory note, are partially visible. The label is from Apace Packaging, LLC.*
FDA Label Image

Label 2 (Screen Shot 2016 03 25 At 3.19.46 Pm)

Label 2 (Screen Shot 2016 03 25 At 3.19.46 Pm)
This image shows a drug-related text panel for UroAv-B, manufactured for Apace Packaging, LLC. It includes storage instructions, precautions about product appearance, contact information for reporting adverse events, and a note to see full prescribing information.*

* 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.