Desmopressin Acetate
Product Images NDC 54868-5602

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Desmopressin Acetate (NDC 54868-5602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, Inc., 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

Desmopressin Acetate Nasal Solution, 0.01% (structural Formula) (35094c6e 1124 461d 9217 Aa4084e044e7 01)

Chemical structure of desmopressin acetate displayed as a peptide sequence with its molecular formula components and associated water molecules.*

FDA Label Image

Figure A (illustration Direction) (35094c6e 1124 461d 9217 Aa4084e044e7 02)

An instructional illustration showing a hand holding a desmopressin acetate nasal spray device, with a focus on pressing the nozzle to administer the spray. The figure is labeled as Figure A.*

FDA Label Image

Desmopressin Acetate Nasal Solution 50 Spray Check-off (35094c6e 1124 461d 9217 Aa4084e044e7 03)

The image is a dose tracking chart for Desmopressin Acetate Nasal Solution, showing numbered check-off boxes from 1 to 50 for spray administration tracking. Instructions advise retaining the chart with the medication, starting with dose #1, checking off after each use, and discarding after 50 sprays.*

FDA Label Image

Desmopressin Acetate Nasal Solution, 0.01% (carton 5ml) (5602)

Label for Desmopressin Acetate 0.01% nasal spray, 5 mL, distributed by Physicians Total Care, Inc. The label includes the product NDC 54868-5602, lot number 0000, and an expiration date of 01/60. Manufactured by Rausch & Lomb Incorporated.*

* 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.