KETOPHENE- ketophene 
California Pharmaceuticals, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

KETOPHENE - 70332-101

Instructions for Preparation
Page 1
Page 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

Ketophehe Kit Instructions 1

Ketophehe Kit Instructions 2

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

RapidPaq Label

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

Ethoxy Diglycol Label

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

Ketoprofen USP Label

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

Ketophene Kit

KETOPHENE 
ketophene kit
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70332-101
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70332-101-011 in 1 KIT01/01/2016
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 33.5 g
Part 21 BOTTLE 33.5 g
Part 31 JAR 100 g
Part 1 of 3
ETHOXYDIGLYCOL 
diethylene glycol monoethyl ether liquid
Product Information
Route of AdministrationTOPICAL
Inactive Ingredients
Ingredient NameStrength
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
133.5 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other
Part 2 of 3
KETOPROFEN 
ketoprofen powder, for suspension
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KETOPROFEN (UNII: 90Y4QC304K) (KETOPROFEN - UNII:90Y4QC304K) KETOPROFEN33.5 g  in 33.5 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
133.5 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other
Part 3 of 3
RAPIDPAQ CREAM BASE 
rapidpaq cream base cream
Product Information
Route of AdministrationTOPICAL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
SORBITOL (UNII: 506T60A25R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1100 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/2016
Labeler - California Pharmaceuticals, LLC (021420944)
Registrant - California Pharmaceuticals, LLC (021420944)
Establishment
NameAddressID/FEIBusiness Operations
California Pharmaceuticals, LLC021420944manufacture(70332-101) , repack(70332-101)

Revised: 7/2016
Document Id: c107b5b2-6eba-429b-a8de-d713b791d3fe
Set id: 271e6176-698a-30dd-e054-00144ff88e88
Version: 4
Effective Time: 20160721
 
California Pharmaceuticals, LLC