Recothrom Kit
Product Images NDC 0338-0326

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Recothrom (NDC 0338-0326). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Recothrom Representative Carton Label 0338-0330-01 2 Of 2 (1170bb13 Dbbb 4929 9cd1 87b590241c29 00)

RECOTHROM thrombin topical recombinant 20,000 units kit packaging label by Baxter Healthcare Corporation. The label highlights it is for topical use only, not for injection, and includes a spray applicator kit. Storage instructions and contents of both the Recothrom kit and spray applicator are listed.*

FDA Label Image

Recothrom Representative Carton Label 0338-0330-01 1 Of 2 (1170bb13 Dbbb 4929 9cd1 87b590241c29 01)

RECOTHROM 20,000 units kit containing thrombin topical recombinant for topical use only. The packaging includes storage instructions, contents of the kit, and manufacturer information for Baxter Healthcare Corporation. It is labeled as prescription-only and specifies spray applicator kit contents.*

FDA Label Image

Recothrom Representative Carton Label 0338-0326-01 3 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 02)

FDA Label Image

Recothrom Representative Carton Label 0338-0326-01 2 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 03)

Packaging label for Recothrom Thrombin Topical (Recombinant) Kit by Baxter Healthcare Corporation. The label indicates a 20,000 unit strength, intended for topical use only, with a storage temperature of 2-25°C (36-77°F). The label includes the NDC code 0338-0326-01 and warnings not to inject the product.*

FDA Label Image

Recothrom Representative Carton Label 0338-0326-01 1 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 04)

RECOTHROM thrombin topical recombinant 20,000 units kit packaging label from Baxter Healthcare Corporation. The label includes storage instructions to keep at 2-25°C (36-77°F) without freezing and warns 'For topical use only - do not inject.' The kit contains one single-use vial of thrombin topical recombinant, diluent, syringes, and transfer devices. NDC 0338-0326-01 is visible.*

FDA Label Image

Recothrom Representative Carton Label 0338-0322-01 3 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 05)

Label for RECOTHROM thrombin topical (recombinant) kit by Baxter Healthcare Corporation. The label shows 5,000 units dosage, warning for topical use only and not to inject. It lists contents including a single-use vial of thrombin, a prefilled diluent syringe, sterile needle-free transfer device, empty syringe for transfer, and syringe label. Storage instructions recommend 2-25°C and avoiding freezing.*

FDA Label Image

Recothrom Representative Carton Label 0338-0322-01 2 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 06)

RECOTHROM 5,000 units kit packaging label showing the brand name and generic name thrombin topical recombinant. The label clearly states 'For topical use only - do not inject' and lists contents including a single-use vial with 5,000 units of thrombin topical recombinant, a prefilled diluent syringe, a needle-free transfer device, an empty syringe for transfer, and a syringe label. Manufactured for Baxter Healthcare Corporation in Deerfield, Illinois, USA.*

FDA Label Image

Recothrom Representative Carton Label 0338-0322-01 1 Of 3 (1170bb13 Dbbb 4929 9cd1 87b590241c29 07)

Packaging label imagery for RECOTHROM, a thrombin topical recombinant human prescription drug kit. The image shows part of the carton design with pink outlines, with no visible text or detailed product information. The labeler is Baxter Healthcare Corporation.*

* 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.