Arnica Relief Cream
Product Images NDC 61727-112

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Arnica Relief (NDC 61727-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Homeocare Laboratories, 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

Arnica Cream Back Pic

This is a description of a product containing Amica Montana 1X as the active ingredient and other inactive ingredients such as avocado oil, Capryl Glycol, Cetyl Alcohol, Dimethicone, Dimethyl Taurate Copolymer, Giycerin USP, Glyceryl Stearate, among others. It is for external use only, safe for children over 2 years old, and should be applied generously to the affected area 2 to 3 times daily until completely absorbed. This product warns users not to get into the eyes, not to apply on open skin, and to stop use and ask a doctor if the condition worsens. It is manufactured and distributed by Homeocare Laboratories, Inc. in Yonkers, NY.*

FDA Label Image

Arnica Cream Front Pic

The text describes a cream named "ARNICA Relief" that is a homeopathic medicine for pain relief and first-aid remedy. It helps in relieving bruises, injuries, muscle aches, and discomfort caused by pre/post surgery. The cream comes in a packaging size of 2 oz (56.70g) and has NDC code 61727-112-02.*

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