Ketophene
FDA Label NDC 70332-101

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by California Pharmaceuticals, Llc for the product Ketophene (NDC 70332-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding instructions for preparationpage 1page 2, rapidpaq™ cream base product label, ethoxy diglycol product label, ketoprofen, usp product label, ketophene kit product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Instructions For Preparationpage 1Page 2

NDC 70332-101-01 For Prescription Compounding Only Rx only

RapidPaq™ Ketophene™

(20% Ketoprofen topical cream kit)

RapidPaq™ kits provide a convenient approach to rapidly prepare prescription medications, as all components are pre-measured. This kit is manufactured according to US FDA current Good Manufacturing Practices (cGMP).

Description:

This kit contains active and inactive materials to prepare approximately 167 grams of ketoprofen topical cream. This kit may only be used for prescription compounding by an appropriate licensed medical professional, in response to a physician's prescription, to create a medication tailored to the specialized needs of an individual patient.

Active Ingredients:

- 33.5 g Ketoprofen, USP

Inactive Ingredients:

- 100 g RapidPaq Cream Base (D.I Water, Cetearyl Alcohol, Cyclomethicone, Polysorbate-60, Sorbitol, Phenoxyethanol(and)ethylhexlglycerin,

Tocopheryl Acetate, Aloe Barbadensis, Disodium EDTA,)

- 33.5 g ethoxy diglycol

- Spatula

-Instructions

Pharmacist instructions for Preparation

1 Remove and Inspect the Contents of the Kit

Ensure that all components are present. Ensure that the safety seals are present on the Ketoprofen, ethoxy diglycol and RapidPaq Cream Base. If components are missing or not intact, do not use the kit.

2 Prepare for Mixing

Wear gloves and eye protection during mixing operations. Remove cap and seal from the RapidPaq Cream Base. Break the seal and remove the cap from the Ketoprofen and ethoxy diglycol.

3 Dissole the Ketoprofen

Transfer approximately 2/3 of the ethoxy diglycol to the Ketoprofen jar. With the supplied spatula, mix them together until they are mostly dissolved. Transfer the Ketoprofen mix to the jar of RapidPaq Cream Base. Transfer the remaining 1/3 of ethoxy diglycol to the Ketoprofen jar and repeat the mixing process. transfer the remaining Ketoprofen mix to the jar of RapidPaq Cream Base.

4 Complete the Mixing Process

Using the spatula, mix the RapidPaq Crean base jar that now contains the ethoxy diglycol and Ketoprofrn ingredients thoroughly for about 2 minutes or until fully dissolved.

5 Relabel the Resulting Cream

Label the resulting topical cream as required for prescription products. Ensure that the original RapidPaq Cream Base label is removed or obscured, since the original label is no longer accurate once the cream is prepared.

Discard the spatula.

Store the unused kit at room temperature of 15-30°C (59-86°F). Once prepared, store the topical cream between 15-30°C (59-86°F). The resulting final topical cream is stable for up to eight weeks.

U.S. Patents Pending

Repacked and Distributed by:

California Pharmaceuticals, LLC

768 Calle Plano

Camarillo, CA 93012

CS113-A1 rev 2

California

PHARMACEUTICALS LLC

Rapidpaq™ Cream Base Product Label

Do not use if seal is broken

California

PHARMACEUTICALS LLC

RapidPaq™ Cream Base

Net contents: 100g

Ingredients: (D.I Water, Cetearyl Alcohol, Cyclomethicone, Polysorbate-60, Sorbitol, Phenoxyethanol(and)ethylhexlglycerin, Tocopheryl Acetate, Aloe Barbadensis, Disodium EDTA

RX Only

Manufactured For California Pharmaceuticals, LLC, Camarillo, CA 93012

Ethoxy Diglycol Product Label

Do not use if safety seal is broken

Ethoxy Diglycol

Diethyl Glycol Monoethly Ether

CAS # 111-90-0

Net contents 33.5 g

Rx Only

Repackaged By;

California Pharmaceuticals, LLC

Camarillo, Ca 93012

California

PHARMACEUTICALS LLC

cs112-A1 rev 1

Ketoprofen, Usp Product Label

Do not use if seal is broken

Ketoprofen, USP

C16H14O3 CAS # 22071-15-4

Net contents: 33.5 g

California

PHARMACEUTICALS

RX Only

Repackaged by California Pharmaceuticals, LLC, Camarillo, CA 93012

CS110-A1 rev 1

Ketophene Kit Product Label

NDC 70332-101-01

Rx only

RapidPaq™

Kit for Topical Cream

KETOPHENE™

(20% ketoprofen cream kit) Non-Steroid Anti-Inflammatory

Store kit at room temperature,

15-30°C (59-86°F0

Description:

This kit contains active and inactive materials to prepare approximately 167 grams of Ketoprofen topical cream. This kit may only be used for prescription compounding by an appropriate licensed medical professional, in response to a physician's prescription, to create a medication tailored to the specialized needs of an individual patient.

Active Ingredients:

- 33.5 g Ketoprofen, USP

Inactive Ingredients:

- 100 g RapidPaq Cream Base (D.l Water, Cetearyl Alcohol, Cyclomethicone, Polysorbate-60, Sorbitol, Phenoxyethanol (and) ethylhexylglycerin,

Tocopheryl Acetate, Aloe Barbadensis, Disodium EDTA)

- 33.5g ethoxy diglycol

- Spatula

- Instrustions

U. S. Patents Pending

Do not use if safety seal is broken

California

PHARMACEUTICALS

Repacked and Distributed By:

California Pharmaceuticals, LLC

768 Calle Plano

Camarillo, CA 93012

CS114-A1 rev 2

* Please review the disclaimer below.