Arnicare Bruise Gel
Product Images NDC 0220-9084

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Arnicare Bruise (NDC 0220-9084). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laboratoires Boiron, 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

Arnicare Bruise Etu.1fs1 04.2020

FDA Label Image

Arnicare Bruise Gel Tua.1fs3

Arnicare Bruise Gel Tua.1fs3
The text appears to be a logo for a product named "BRUISE RELIEF" with a subtext "Arnicare". There is no additional readable text available.*
FDA Label Image

Arnicare Bruise Tua.1fs3 05.2020

FDA Label Image

Boxes (Box)

Boxes (Box)
Arnicare Bruise Relief is a homeopathic medicine used for the reduction of pain, swelling, and discoloration caused by bruises. The active ingredient, Arnica montana, is a naturally occurring plant extract, and its effectiveness is supported by the Homeopathic Pharmacopoeia of the United States. The medication is designed to be quickly absorbed through the skin, and the gel is non-greasy and unscented. The product is paraben-free, and the user should apply a thin layer to the affected area and massage gently for maximum effectiveness. The medication should be used only as directed and kept out of reach of children. If you are allergic to any active or inactive ingredient, or the bruising condition worsens, you should immediately stop using the medication and consult a doctor.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.