Promethazine Hydrochloride Solution
Product Images NDC 81033-016

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Promethazine Hydrochloride (NDC 81033-016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corporation, 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
FDA Label Image
FDA Label Image

Ndc 81033-016-50 (Promethazine 5ml Carton Label)

Ndc 81033-016-50 (Promethazine 5ml Carton Label)
Label for Promethazine Oral Solution, USP 6.25 mg/5 mL by Kesin Pharma Corporation. The label includes the NDC 81033-016-50, a barcode, lot number K0000000, and an expiration date of November 19, 2024. It indicates the product is for institutional use only and distributed by Kesin Pharma Corporation, Oldsmar, FL, packaged as 50 unit dose cups.*
FDA Label Image

Ndc 81033-016-05 (Promethazine 5ml Foil)

Ndc 81033-016-05 (Promethazine 5ml Foil)
Promethazine Hydrochloride Oral Solution 6.25 mg per 5 mL in a unit-dose blister packaging. The label states it delivers 5 mL and contains 7% alcohol. It is packaged by Kesin Pharma Corporation, Oldsmar, FL, with storage instructions to keep between 68°F and 77°F and protect from light. The NDC number 81033-016-05 is printed along with a barcode.*
FDA Label Image

Chemical-structure (Promethazine Str)

Chemical-structure (Promethazine Str)
Chemical structure diagram of promethazine hydrochloride showing its molecular structure including aromatic rings and side chains, with an HCl group indicating the hydrochloride salt form.*

* 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.