My Way
Product Images NDC 43386-620

3 FDA label images from Gavis Pharmaceuticals, Llc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for My Way (NDC 43386-620). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gavis Pharmaceuticals, 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

07b96626-figure-01 (07b96626 Figure 01)

07b96626-figure-01 (07b96626 Figure 01)
Chemical structure diagram of the active ingredient corresponding to the product My Way by GAVIS Pharmaceuticals, LLC. The structure shows a multi-ring steroid-like compound with hydroxyl and ketone groups, methyl substitutions, and a side chain containing an aldehyde group.*
FDA Label Image

07b96626-figure-02 (07b96626 Figure 02)

07b96626-figure-02 (07b96626 Figure 02)
Packaging label for My Way levonorgestrel tablet 1.5 mg by GAVIS Pharmaceuticals. The label shows this is an emergency contraceptive tablet with a caution that it is Rx only for women younger than age 17 and is not for regular birth control. The package includes one tablet of levonorgestrel 1.5 mg.*
FDA Label Image

07b96626-figure-03 (07b96626 Figure 03)

07b96626-figure-03 (07b96626 Figure 03)
My Way Levonorgestrel Tablet 1.5 mg packaging label from GAVIS Pharmaceuticals, LLC. The label identifies the product as an emergency contraceptive for women younger than age 17. It highlights that one tablet equals one dose and emphasizes usage within 72 hours after unprotected sex. The label also states this is not for regular birth control.*

* 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.