Thiamine Hydrochloride Injection, Solution
Product Images NDC 70756-684

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Thiamine Hydrochloride (NDC 70756-684). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma 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

Structure (D00087d1 1205 4b02 972a 80d7ee48c930 01)

Chemical structure of Thiamine Hydrochloride showing its molecular formula C12H17ClN4OS and molecular weight of 337.3. The structure includes a thiazole ring and a pyrimidine ring with functional groups as part of the compound.*

FDA Label Image

Vial Label (D00087d1 1205 4b02 972a 80d7ee48c930 02)

Label for Thiamine Hydrochloride Injection, USP 200 mg per 2 mL (100 mg/mL) in a 2 mL multi-dose vial for intramuscular or intravenous use. The label shows the manufacturer as Lifestar Pharma LLC, with the product made in India. It includes storage instructions to protect from light, a barcode, and placeholders for expiration date and lot number.*

FDA Label Image

Carton Label (D00087d1 1205 4b02 972a 80d7ee48c930 03)

Packaging label for Thiamine Hydrochloride Injection, USP 200 mg per 2 mL (100 mg/mL) solution by Lifestar Pharma LLC. The label indicates intramuscular or intravenous use, packaged as 25 multi-dose vials of 2 mL each. The label includes storage instructions, sterilization details, and manufacturer information including origin in India and a barcode.*

* 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.