Aplicare Povidone-iodine
Product Images NDC 52380-0001

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Aplicare Povidone-iodine (NDC 52380-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aplicare Products, 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.

FDA Label Image

Epinephrine Structural Formula (Epinephrine Injection)

Chemical structure of the active ingredient shown in the image, depicting a benzene ring with hydroxyl groups and attached side chains including a hydroxyl group (OH), hydrogen (H), and a methylated amino group (CH2NHCH3).*

FDA Label Image

Epinephrine Pack Label (Epinephrine Pack Label)

Label showing information for Epinephrine Injection, USP, 1:1000 (1 mg/mL) in a 1 mL injectable dosage form. The label includes the NDC 0409-7241-61 and the manufacturer Hospira, Inc., Lake Forest, IL. The label also shows a barcode, expiration date of 1 DEC 2012, and indicates the product is for SQ/IM use and prescription only.*

FDA Label Image

Lidocaine Pack Label (Lidocaine Pack Label)

Packaging label showing Lidocaine HCl Injection, USP 1% (10 mg/mL) in a 5 mL preservative-free vial. The label includes the NDC 0409-4713-65, lot number 931153A, and expiration date of 1 SEP 2013. The manufacturer is Hospira, Inc., Lake Forest, IL, USA. The Hospira logo is also visible.*

FDA Label Image

Povidone Iodine Solution (Povidone Iodine Solution)

Aplicare Povidone-Iodine antiseptic solution package containing 0.75 fluid ounces (22.5 mL). The front label shows the brand name Aplicare and the active ingredient Povidone-Iodine USP 10%. The back label includes drug facts, warnings, directions for use, inactive ingredients, contact information, and storage instructions. The package is single-use and sterile unless opened or damaged.*

FDA Label Image

V49663c-25 (V49663c 25)

Label for Spinal 25G Pencil Point needles by Novaplus, manufactured by Smiths Medical ASD, Inc. The label lists procedural and prep components including various needles, syringes, sponges, and a povidone-iodine solution. It includes safety warnings, handling instructions, and sterilization information. The packaging features a barcode, storage instructions, and regulatory symbols.*

FDA Label Image

Lidocaine Hydrochloride Injection (Lidocaine Hydrochloride Injection Figure 1)

Chemical structure diagram showing a molecular formula with a benzene ring substituted with two methyl groups, an acetamide linked to an ethylamine derivative, hydrochloride, and water components. This likely represents the active ingredient or a related compound associated with Aplicare Povidone-Iodine.*

FDA Label Image

Marcaine Figure 1 (Marcaine Figure 1)

Chemical structure of the active ingredient in Aplicare Povidone-Iodine, showing a nitrogen-containing ring connected to an amide group and a dimethyl-substituted benzene ring, with associated hydrochloride and water molecules.*

FDA Label Image

Marcaine Figure 2 (Marcaine Figure 2)

Chemical structure diagram depicting the molecular formula of an active ingredient, showing a sugar-like ring with hydroxyl groups and an attached water molecule, indicating a hydrate form.*

FDA Label Image

Marcaine Figure 3 (Marcaine Figure 3)

Label for Marcaine Spinal 2 mL, a bupivacaine hydrochloride in dextrose injection, USP. The label includes drug quantity details, NDC 0409-1761-62, and manufacturer Hospira, Inc., Lake Forest, IL. It specifies the drug is for spinal use only and requires a prescription.*

* 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.