Nightly Face Treatment - Dimethicone
Product Images NDC 71593-101

View Photos of 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 Nightly Face Treatment - Dimethicone (NDC 71593-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Arg Laboratories Inc, 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

Nsc.adv.nc.carton.30ml.unv.v7_page_1 (Nsc.adv.nc.carton.30ml.unv.v7 Page 1)

Nsc.adv.nc.carton.30ml.unv.v7_page_1 (Nsc.adv.nc.carton.30ml.unv.v7 Page 1)
Label for NIGHTLY FACE TREATMENT - DIMETHICONE by ARG LABORATORIES INC featuring Nerium SkinCare Inc. The front shows the product name with Dimethicone as the active ingredient and mentions patented Nerium Oleander Extract. The label includes detailed drug facts such as active ingredient concentration (1.5%), uses, warnings, directions, inactive ingredients, storage instructions, and contact information for manufacturer and distributor. It also highlights key ingredients and states dermatologist testing. The quantity is 30 mL (1 fl. oz.).*
FDA Label Image

Nsc.neriumrx.nc.carton.30ml.usa.hk.tk.kw.v12.lr_page_1 (Nsc.neriumrx.nc.carton.30ml.usa.hk.tk.kw.v12.lr Page 1)

Nsc.neriumrx.nc.carton.30ml.usa.hk.tk.kw.v12.lr_page_1 (Nsc.neriumrx.nc.carton.30ml.usa.hk.tk.kw.v12.lr Page 1)
Drug Facts panel for NIGHTLY FACE TREATMENT - DIMETHICONE with active ingredient Dimethicone 1.5% as a skin protectant. The label includes uses, warnings, directions, and inactive ingredients in multiple languages. It also lists key ingredients, manufacturer, importer, distributor information, and contact numbers, all on a red background.*

* 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.