P-BLOC

Drug Labeling and Warnings

Drug Details [pdf]

P-BLOC - sarraceniaceae injection 
Creative Science, 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.

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P-BLOC

NDC: 53413-752-01

P-Bloc®

NET CONTENTS: 100 mL

CAUTION: Federal Law Prohibits Dispensing without Prescription.

Manufactured for:
CREATIVE SCIENCE LLC
455 SOVEREIGN CT
BALLWIN, MO 63011 USA

Lot No.:              Exp. Date:

STERILE - MULTIPLE DOSE VIAL
An injectable source of the volatile salts of Pitcher Plant (Sarraceniaceae) with 5% w/v Ethanol as a solution aide and
0.75% w/v Benzyl Alcohol as a preservative.

USAGE: P-Bloc™ sterile aqueous solution is indicated for the temporary relief of symptoms
associated with neurologic pain.

DOSAGE AND ADMINISTRATION: Paravertebral injections should be observed as follows: Local infiltration 5-10 mL,
Caudal Canal 10 mL, Sciatic Nerve 10 mL, Cervical 2-3 mL, Dorsal 5-10 mL, Lumbar 5-10 mL, Sacral 3-5 mL.

CAUTION: Caution should be exercised during injection.  Procedure should be done slowly. P-Bloc™ should not be
used in areas of local inflammation. Keep out of reach of children.

WARNINGS: There may appear localized and usually transient side effects resulting in a heat sensation or aggravated
symptoms.  Withdraw plunger of syringe to make sure the needle point is not in a blood vessel.  Injection should be made through
a procaine wheal.

CONTRAINDICATIONS: P-Bloc™ is contraindicated in areas of local inflammation.

Store between 15°and 30°C (59° and 86°F).

Rev 10/12

P-BLOC  
sarraceniaceae injection

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 53413-752
Route of Administration	PARENTERAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SARRACENIA PURPUREA (UNII: FOP08H143P) (SARRACENIA PURPUREA - UNII:FOP08H143P)	SARRACENIA PURPUREA	12.5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53413-752-01	100 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product	11/20/2004

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/20/2004	07/01/2019

Labeler - Creative Science, LLC (010785170)

Revised: 8/2019

Document Id: f6aa6a42-8506-47f6-9160-e047cd768b99

34391-3

Set id: aad16dc1-aa6a-4ff8-a0e9-43d30e0da265

Version: 5

Effective Time: 20190815