Ozobax Solution
Product Images NDC 69528-302

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ozobax (NDC 69528-302). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rosemont 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

302-08 (302 08)

302-08 (302 08)
This is a description for an oral solution called Baclofen. Each 5 mL of the solution contains 10 mg of baclofen. The recommended dosage should be obtained from the prescribing information. The solution should be dispensed in a container with a child-resistant closure and kept in a cool place between 20°C to 25°C (66°F to 77°F), with excursions allowed to 15°C to 30°C (59°F to 86°F). The solution is tamper evident with a seal under the cap, which should not be used if broken or missing. The solution contains inactive ingredients such as glycerin, methylparaben, propylparaben, purified water, and sucralose. It may also contain sodium hydroxide or hydrochloric acid for pH adjustment. The solution is available in different concentrations and comes in a clear liquid form in a 237 mL (8 fl.oz.) container. It is manufactured in Canada by Metacel Pharmaceuticals LLC and has an NDC code of 69528-302-08. Additional information such as lot number, expiration date, and a serial number is not available.*
FDA Label Image

302-16 (302 16)

302-16 (302 16)
Each 5 mL of this oral solution contains 10 mg of baclofen. This medication is typically used for muscle spasms and is available in different concentrations. It should be stored in a light-resistant container with a child-resistant closure. The recommended dosage should be obtained from the prescribing information. It is important to keep this medication out of reach of children. The oral solution has inactive ingredients such as glycerin, methylparaben, propylparaben, purified water, and possibly sodium hydroxide or hydrochloric acid for pH adjustment. The solution is clear and comes in a 473 mL bottle. It is tamper-evident with a foil seal under the cap. Do not use if the foil seal is broken or missing. The product is manufactured in Canada by Metacel Pharmaceuticals LLC and the lot and expiration date can be found on the packaging.*
FDA Label Image

Bac Structure (Bac Structure)

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