Acunivive 90
Product Images NDC 70529-122

3 FDA label images from It3 Medical 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 Acunivive 90 (NDC 70529-122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by It3 Medical 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

Acunivive 90 Kit Components (Acunivive 90 Componentlabel)

Acunivive 90 Kit Components (Acunivive 90 Componentlabel)
Packaging label featuring Ketorolac Tromethamine Injection, USP in two strengths: 30 mg/mL in a 1 mL single-dose vial and 60 mg/2 mL in a 2 mL single-dose vial. Labels indicate intramuscular or intravenous use, with product details including lot and expiration dates. Also includes a label for McKesson Alcohol Prep Pad, sterile, saturated with 70% isopropyl alcohol, measuring 1.2" x 2.6" (3 cm x 6.5 cm).*
FDA Label Image

Acuniv-90 (Acunivive 90 Kit Label)

Acuniv-90 (Acunivive 90 Kit Label)
Label for Acunivive 90 Injection System by IT3 Medical LLC with product NDC 70529-122-90. The label lists contents including Ketorolac Tromethamine in two vial sizes, syringes, needles, a Luer Tip cap, gauze sponge, sterile square bandage, and alcohol prep pads. Storage instructions advise cool dry storage at 25°C (77°F) with permitted excursions to 15-30°C (59-86°F). Additional instructions and manufacturer contact information are also present.*
FDA Label Image

Image Description (Keth Formula)

Image Description (Keth Formula)
Chemical structure of Acunivive 90's active ingredient, depicting its molecular components including a benzene ring, a pyrrolidine ring, and multiple hydroxyl groups.*

* 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.