Albutein Injection, Solution
Product Images NDC 68516-5215

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Albutein (NDC 68516-5215). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grifols Usa, 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.

Product Images & Figures Index

FDA Label Image

100 mL Bag Label (100 mL Bag Label)

100 mL Bag Label (100 mL Bag Label)
This is a prescription-only medication called ALBUTEIN FlexBag 20% containing 20 grams of Albumin (Human) in aqueous diluent. It is used for intravenous administration and is stabilized with sodium caprylate and sodium acetyl tryptophanate. There are no preservatives in this medication, and it is heat-treated at 60°C for 10 hours. The sodium range is 130-160 mEq/L, and the medication comes in a single-dose container. You should always check the bag for leaks before use and discard any bag that has compromised sterility. It is essential to keep the medication at temperatures below 30°C and not allow it to freeze. This medication is manufactured by Grifols Biologicals LLC in Los Angeles, USA.*
FDA Label Image

100 mL Carton Back (100 mL Carton Back)

100 mL Carton Back (100 mL Carton Back)
ALBUTEIN FlexBag™ is a 20% solution of human albumin used for intravenous administration. It contains 20 grams of human serum albumin per 100 mL and is stabilized with sodium capofate and sodium aceyltyptophanate. The solution has no preservatives and has been heat-treated at 60°C for 10 hours. It is important to discuss the risks and benefits of this product with a healthcare provider before use. Prior to administration, check the bag for leaks and discard if found. Do not use if cloudy or discolored. Store at temperatures below 30°C and do not freeze. Grifols Biologicals LLC manufactures this product and is located in Los Angeles, California.*
FDA Label Image

100 mL Carton Front (100 mL Carton Front)

100 mL Carton Front (100 mL Carton Front)
FDA Label Image

50 mL Bag Label (50 mL Bag Label)

50 mL Bag Label (50 mL Bag Label)
ALBUTEIN FlexBag™ 20% is an intravenous solution containing 10 grams of Albumin (Human) in aqueous diluent, with sodium range of 130-160 mEq/L, stabilized with sodium caprylate and sodium acetyltryptophanate, and heat-treated at 60 °C for 10 hours. It is a single-dose container meant for administration after checking for leaks and absence of turbidity. Administration should not start more than 4 hours after opening the container. Any unused contents and devices must be discarded after use. The solution should be stored at temperatures not exceeding 30 °C without allowing freezing and keeping the overwrap intact.*
FDA Label Image

50 mL Carton Back (50 mL Carton Back)

50 mL Carton Back (50 mL Carton Back)
This appears to be a description of a medical product called "ALBUTEIN FlexBag™ 20%" used for intravenous administration. The product is made up of human albumin in an aqueous diluent and is intended to be isotonic with plasma. The solution is stabilized with sodium caprate and sodium acetofluorotryptophanate and contains no preservatives. The patient and physician are advised to discuss the benefits and risks before use. The bag should be checked for leaks before administration and discarded if any are found. The unused contents should be discarded, and the product should not be frozen or exposed to temperatures greater than 30°C. The manufacturer is Grifols Biokgials LLC based in Los Angeles.*
FDA Label Image

50 mL Carton Front (50 mL Carton Front)

50 mL Carton Front (50 mL Carton Front)
Albumin (Human) U.S.P. in a solution containing 10 g with 50 mL is available in ALBUTEIN FlexBag™ 20%. It has unique combination for treating surgical, trauma, and burn patients. It is important to store the solution at temperatures not exceeding 30 degrees. Do not allow freeze and ensure the overwrapping intact. The NDC code for the solution is 68516-5215-7. The rest of the text is not useful and appears to be random characters.*
FDA Label Image

Figures 1-4 (Figs1 4.jpt)

Figures 1-4 (Figs1 4.jpt)

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