Camphor Spirit Liquid
Product Images NDC 82645-920

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Camphor Spirit (NDC 82645-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharma Nobis, 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.

FDA Label Image

Ddm (046792082 Ddm Camphor Spirit 2oz Web)

The image shows the Drug Facts label for Camphor Spirit USP liquid, an OTC topical product containing Camphor 10% as a counterirritant and 84% alcohol. It includes warnings for external use only, directions for use, inactive ingredients, flammability caution, and contact information for the distributor, Drug Mart-Food Fair.*

FDA Label Image

Qc (L046792066 Qc Camphor Spirit)

Drug Facts panel for Camphor Spirit USP 10% topical liquid showing active ingredient as Camphor 10% labeled as an external analgesic. It includes indications for minor aches and pain, warnings about proper use and avoiding ingestion, directions for application diluted with olive oil, flammability notice, and inactive ingredients Alcohol 84% and Purified Water. Distributed by C.D.M.A., Inc.*

FDA Label Image

Label (L046794074 Sm Camphor Spirit)

Label for Camphor Spirit USP 10% (Camphor 100 mg/mL) topical liquid by Pharma Nobis, LLC. The label prominently shows the product name with a red section indicating 84% alcohol content as a counterirritant, a danger poison warning, and includes a Drug Facts panel detailing active ingredient, uses, warnings, and directions. The container size is 2 fluid ounces (59 mL). The labeler is identified as McKesson, San Francisco, CA.*

FDA Label Image

Ldrcam.jpg (Ldrcam)

Drug Facts panel of Camphor Spirit USP 10% topical liquid, containing active ingredient Camphor 10% as an external analgesic. The label includes indications for temporary relief of minor aches and pains, warnings for external use only, and directions for dilution and application. It also mentions storage instructions, flammability, and poison control contact information.*

* 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.