Fluticasone Propionate Spray, Metered
Product Images NDC 60429-195

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Fluticasone Propionate (NDC 60429-195). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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.

Product Images & Figures Index

FDA Label Image

Approved (Fluticasone Propionate Nasal Spray)

Approved (Fluticasone Propionate Nasal Spray)
This is a description for Fluticasone Propionate Nasal Spray, which has 50mcg per spray and comes in a 16g net fill weight bottle. The bottle contains 120 metered sprays, each containing 50mcg of Fluticasone Propionate. The nasal spray is for intranasal use only, and it is important to read the accompanying directions before use. The packaging insert provides dosage and administration instructions. The carton contains cleaning instructions. The nasal spray should be stored between 4°C and 30°C and should be shaken gently before use. The manufacturer is Agotexinc and is distributed by WBLTT.*
FDA Label Image

Box_page_1.jpg (Box Page 1)

Box_page_1.jpg (Box Page 1)
This is a description of Fluticasone Propionate Nasal Spray. It is a prescription medication indicated for intranasal use only. Each bottle contains 16 g net fill weight and 120 metered sprays. The nasal spray contains 50 mcg of fluticasone propionate per spray. It is necessary to prime the pump before the first use, and shake the bottle gently before each use. The bottle should be stored at a temperature of 4°-30°C. The nasal spray contains an aqueous suspension with benzalkonium chloride, dextrose, microcrystalline cellulose and carboxymethylcellulose sodium, phenylethyhlcohol, polysorbate 80 and purified water. The pharmacist should detach patient instructions from prescribing information along perforation and dispense with prescription. The manufacturer is Apotex Inc. in Canada and it is marketed by GSMS, Incorporated in the USA. The dosage and administration instructions indicate that the nasal spray should be cleaned once a week and provides instructions on how to do so.*
FDA Label Image

Figure-1.jpg (Figure 1)

Figure-1.jpg (Figure 1)
This appears to be a document containing only a few words and an image, indicating a nasal applicator with a dust cover. No further information is available.*
FDA Label Image

Figure-2.jpg (Figure 2)

Figure-2.jpg (Figure 2)
FDA Label Image

Figure-3.jpg (Figure 3)

Figure-3.jpg (Figure 3)
FDA Label Image

Figure-4.jpg (Figure 4)

Figure-4.jpg (Figure 4)
FDA Label Image

Figure-5.jpg (Figure 5)

Figure-5.jpg (Figure 5)
FDA Label Image

Figure-6.jpg (Figure 6)

Figure-6.jpg (Figure 6)
FDA Label Image

Structure-01 (Fluticasone 01)

Structure-01 (Fluticasone 01)

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