Ketophene
Product Images NDC 70332-101

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Ketophene (NDC 70332-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by California Pharmaceuticals, 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

Ketoprofen Usp Label (Ketophene Cs110 A1 Rev 1)

Ketoprofen Usp Label (Ketophene Cs110 A1 Rev 1)
This is a description of a medication called Ketoprofen, USP. The chemical formula and CAS number are provided. The net contents are given as 33.5 9. The medication has been repackaged by California Pharmaceuticals, LLC in Camarilo, CA. No information on usage, benefits or side effects is provided.*
FDA Label Image

Ethoxy Diglycol Label (Ketophene Cs112 A1 Rev 1 Label Ethoxy Dig)

Ethoxy Diglycol Label (Ketophene Cs112 A1 Rev 1 Label Ethoxy Dig)
This is a warning label on a product advising not to use it if the safety seal is broken. The product contains Ethoxy Diglycol and Diethyl Giycol Monosthyl Ether, and is intended only for prescription use. The CAS number is listed as 111-900, and it has a net content of 33.5. The product was repackaged by California Pharmaceuticals, LLC and is located in Camarillo, California. There is a reference number of CSt2-A rev 1.*
FDA Label Image

Ketophehe Kit Instructions 1 (Ketophene Cs113 A1 Instructions 1)

Ketophehe Kit Instructions 1 (Ketophene Cs113 A1 Instructions 1)
RapidPaq Ketophene is a prescription compounding kit that contains active and inactive ingredients to prepare approximately 167 grams of ketoprofen topical cream. It is manufactured according to US FDA current Good Manufacturing Practices (cGMP). The kit is pre-measured with all components and can only be used by licensed medical professionals in response to a physician's prescription to cater to individual patients' specialized needs. The kit includes a spatula and instructions for preparation. Wear gloves and eye protection during mixing operations, and ensure all components are present and safety seals are intact before use.*
FDA Label Image

Ketophehe Kit Instructions 2 (Ketophene Cs113 A1 Instructions 2)

Ketophehe Kit Instructions 2 (Ketophene Cs113 A1 Instructions 2)
This is a set of instructions for preparing a topical cream used for prescription compounding purposes called "RapidPaq Ketophene," which contains 20% Ketoprofen. The process involves dissolving Ketoprofen in ethoxy diglycol and mixing it with RapidPaq Cream Base. The resulting cream needs to be relabeled for prescription use, and the original label needs to be removed. The kit needs to be stored at room temperature, and the resulting cream is stable for up to eight weeks. The product is repacked and distributed by California Pharmaceuticals, LLC.*
FDA Label Image

Ketophene Kit (Ketophene Cs114 A1 Principle Label Ketophene)

FDA Label Image

Rapidpaq Label (Ketophene Cream Base Cs88 A1 Rev 1)

Rapidpaq Label (Ketophene Cream Base Cs88 A1 Rev 1)
This appears to be a label for a product called California RapidPaq Cream Base. The label warns not to use if the seal is broken. The net content is 1009, although it is unclear what unit of measurement is being used. The ingredients include Catm Rl Cydomticon and Poysres 8. This product was manufactured for California Pharmaceuticas, LLC in Camario, CA 93012.*

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