Ketorolac Tromethamine Solution
Product Images NDC 70512-790

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ketorolac Tromethamine (NDC 70512-790). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sola Pharmaceuticals, 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

10ml Carton (10ml Carton)

This text provides information about a medication containing ketorolac tromethamine for ophthalmic use. It includes details about the composition, dosage instructions, storage guidelines, manufacturer information, and a prescription-only note. The medication is intended for topical ophthalmic use, and the text also mentions batch overprinting and the specific details that will be printed on the packaging during online packing.*

FDA Label Image

10ml Label (10ml Label)

This text provides information about an ophthalmic solution containing ketorolac tromethamine 0.5% as the active ingredient and benzalkonium chloride 0.01% as the preservative. The usual dosage is one drop four times a day, and it should be stored at 20° - 25°C (68° - 77°F) away from light. The solution is for topical ophthalmic use only. The product is manufactured for SOLA Pharmaceuticals and the NDC is 70512-790-10. The text also includes a lot number, manufacturing location in Baton Rouge, LA, and an expiration date.*

FDA Label Image

3ml Carton (3ml Carton)

Description: This is a product information sheet for a 0.1% Ketorolac Tromethamine Ophthalmic Solution. The text includes details on the inactive ingredients, dosage instructions, storage recommendations, and a caution to keep the product out of reach of children. The lot number, expiration date, and packaging details are also mentioned for traceability and quality control.*

FDA Label Image

70512-790*03 3ml (3ml Label)

This is a prescription medication for topical ophthalmic use only. It contains ketorolac tromethamine 0.5% as the active ingredient and benzalkonium chloride 0.01% as a preservative. The usual dosage is one drop four times a day. It should be stored at 20°C - 25°C and protected from light. Manufactured for SOLA Pharmaceuticals in Baton Rouge, LA, and made in India. The NDC number for this product is 70512-790-03. Please refer to the package insert for more information.*

FDA Label Image

5ml Carton (5ml Carton)

This is the description: The text contains information about a medication with active ingredient ketorolac tromethamine 0.5% for ophthalmic use. It provides details on storage conditions, dosage instructions, batch overprinting specifications, and manufacturer details. The medication is stored at 20° - 25°C and should be protected from light. The NDC code for the product is 70512-790-05. The solution is manufactured for SOLA Pharmaceuticals and made in India. Please refer to the package insert for usual dosage instructions. The overprinting specifications include 2D code, GTIN, lot number, and expiration date details printed during online packing.*

FDA Label Image

5ml Label (5ml Label)

This is an eye drop solution containing ketorolac tromethamine at a concentration of 0.5% as the active ingredient and benzalkonium chloride at 0.01% as the preservative. The recommended dosage is one drop administered four times a day. The product is stored at a temperature range of 20-25°C and is manufactured by SOLA Pharmaceuticals in Baton Rouge, LA. The packaging states that the bottle is filled to half capacity. The item has an NDC code of 70512-790-05 and is labeled for prescription use only.*

FDA Label Image

Structural Formula (Structual Formulaa)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.