Sodium Tetradecyl Sulfate Injection, Solution
Product Images NDC 51662-1562

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Tetradecyl Sulfate (NDC 51662-1562). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Labeling (Serialized Labeling)

Sotradecol 1% (sodium tetradecyl sulfate injection) 20 mg/2 mL (10 mg/mL) intravenous injection in a multiple-dose vial. The vial label includes the NDC 67457-162-00, directions for intravenous use only, and is distributed by HF Acquisition Co., LLC, Mukilteo, WA. The label also advises not to use if precipitated and notes Rx only status.*

FDA Label Image

Structure (Structure)

Chemical structure of sodium tetradecyl sulfate, showing its molecular formula with various carbon and oxygen groups, including the sodium (Na) ion, depicted in a structural diagram format.*

FDA Label Image

Vial 1 (Vial Label Part 1)

A label showing manufacturer information for Mylan Institutional LLC in Rockford, IL, USA. The label includes a barcode, a lot number 201218, and an expiration date of May 2023. The label appears to be from the packaging of Sodium Tetradecyl Sulfate injection solution, 10 mg/mL, by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Vial 2 (Vial Label Part 2)

The image shows a vial label for Sotradecol 1% (sodium tetradecyl sulfate injection) by Mylan. The label states the strength as 20 mg/2 mL (10 mg/mL) and specifies it is for intravenous use only. It is Rx only and mentions not to use if precipitated. The vial is a multiple-dose type.*

* 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.