Novarnica
Product Images NDC 61871-001

2 FDA label images from Xcentrik Inc. · 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 Novarnica (NDC 61871-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xcentrik 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

4.06 Fl Oz (120 mL) (Novarnica 120ml)

4.06 Fl Oz (120 mL) (Novarnica 120ml)
Drug Facts panel for Novarnica Pain Relieving Spray by Xcentrik Inc. It lists active ingredients camphor 4% and menthol 8% as topical analgesics. Includes uses for minor aches, simple backache, arthritis, strains, bruises, and sprains. Warnings cover external use only, allergy alert, flammability, and precautions for pregnant or breastfeeding individuals. Directions advise use for adults and children 12 years and older. Additional information includes inactive ingredients, storage, and manufacturer contact details.*
FDA Label Image

2.19 Fl Oz (65 mL) (Novarnica 65ml)

2.19 Fl Oz (65 mL) (Novarnica 65ml)
Drug Facts panel for Novarnica Pain Relieving Spray with natural ingredients by Xcentrik Inc. Lists active ingredients camphor 4% and menthol 8% as topical analgesics. Includes directions for use, inactive ingredients, warnings, and storage information. Highlights uses for temporary relief of minor muscle and joint pain including backache, arthritis, strains, bruises, and sprains. Provided manufacturer contact and product volume of 2.19 FL OZ (65 ml).*

* 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.