Econtra One-step Tablet
Product Images NDC 50102-211

2 FDA label images from Afaxys Pharma, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Econtra One-step (NDC 50102-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Afaxys 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (1.5 mg (6 Blister Carton Label))

Package Label-principal Display Panel (1.5 mg (6 Blister Carton Label))
Packaging label for EContra One-Step 1.5 mg tablet, an emergency contraceptive containing Levonorgestrel. The label shows the product name, dosage form, and strength on multiple panels. Manufactured for Afaxys Pharma, LLC and by Aurobindo Pharma Limited, made in India. The label includes drug facts, usage directions, warnings, and inactive ingredients. The package contains 3 mono cartons of 1 tablet each and is marked as not child-resistant.*
FDA Label Image

Package Label-principal Display Panel (1.5 mg (6 Blister Carton Label))

Package Label-principal Display Panel (1.5 mg (6 Blister Carton Label))
Packaging label for EContra One-Step 1.5 mg (Levonorgestrel) oral tablet by Afaxys Pharma, LLC. The emergency contraceptive label features the product name prominently in blue with the dosage strength. The label includes Drug Facts, warnings, directions, and manufacturer information. The package is marked as containing single-dose tablets with a total of six individual cartons each containing one tablet. NDC 50102-211-16 is shown along with barcode and lot identification details.*

* 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.