Kenalog-80 Injection, Suspension
Product Images NDC 0003-0315

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Kenalog-80 (NDC 0003-0315). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E.r. Squibb & Sons, L.l.c., 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

Kenalog Struct

Chemical structure of triamcinolone acetonide, the active ingredient in KENALOG-80 injection suspension, showing a complex steroid skeleton with hydroxyl, keto, fluoro, and acetonide functional groups.*

FDA Label Image

Kenalog40 10ml Carton Lbl

KENALOG-40 (triamcinolone acetonide injectable suspension, USP) 400 mg per 10 mL (40 mg/mL) vial label. The label shows dosage form as injectable suspension and specifies use for intramuscular or intra-articular administration. The product is manufactured by E.R. Squibb & Sons, L.L.C. and includes storage instructions and a barcode along with dosage and handling warnings.*

FDA Label Image

Kenalog40 1ml Carton Lbl

KENALOG-40 (triamcinolone acetonide injectable suspension, USP) 40 mg per mL single-dose vial label. The label displays dosing information, storage instructions to keep at controlled room temperature 20 to 25°C and protect from freezing, and cautions for intramuscular or intra-articular use only. Manufacturer is Bristol-Myers Squibb Company, Product of Spain.*

FDA Label Image

Kenalog40 5ml Carton Lbl

KENALOG-40 (Triamcinolone acetonide injectable suspension, USP) 40 mg/mL injection, suspension, USP in a 5 mL multiple-dose vial. Provided by E.R. Squibb & Sons, L.L.C., the label includes dosage strength of 200 mg per 5 mL, storage instructions, and specifies use for intramuscular or intra-articular administration only. Contains warnings about controlled room temperature storage and to not use if seal is broken or missing.*

FDA Label Image

Kenalog80 1ml Carton Lbl

The packaging label for KENALOG-80 injection, suspension containing triamcinolone acetonide at 80 mg per mL strength. It is a 1 mL single-dose vial labeled for intramuscular or intra-articular use. The label includes the NDC 0003-0315-05 and identifies E.R. Squibb & Sons, L.L.C. as the manufacturer. Storage instructions and cautionary details about use and shaking before injection are also printed.*

FDA Label Image

Kenalog80 5ml Carton Lbl

Label for KENALOG-80 (triamcinolone acetonide) injection suspension, 80 mg/mL strength. The label shows the dosage of 400 mg per 5 mL in a 5 mL multiple-dose vial for intra-articular or intramuscular use only. Manufactured by E.R. Squibb & Sons, L.L.C., it includes storage instructions, usage warnings, and a barcode with NDC 0003-0315-20.*

* 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.