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0.3 ml AMMONIA INHALANT

A RESPIRATORY STIMULANT

FOR INHALATION ONLY
PRINCIPAL DISPLAY PANEL - VIAL LABEL
1mL NDC 0003-0293-05

Rx only

40mg

KENALOG-40®

Triamcinolone Acetonide

Injectable Suspension, USP
PRINCIPAL DISPLAY PANEL - PREP PAD LABEL
PDI®

REORDER NO. C124

NDC 10819-3883-3

Povidone-Iodine
Prep Pad

Antiseptic/Germicide LARGE

For Professional and Hospital Use

Professional Disposables International, Inc.

Orangeburg, NY 10962-1376 · USA · 1-800-999-6423

www.pdipdi.com Made in USA

1 Prep Pad [1.7 x 3.5 in (4.4 x 8.8 cm)]
PRINCIPAL DISPLAY PANEL - SYRINGE LABEL
2mL NDC 0409-4713-32

Preservative-Free Rx only

1% LIDOCAINE HCl

Injection, USP

10 mg/mL

RL-1045 (11/04)
HOSPIRA, INC., LK. FOREST, IL 60045 USA

PRINCIPAL DISPLAY PANEL – KIT LABEL
NDC 76420-524-01 Rx-Only

Physicians EZ Use
Joint, Tunnel, and Trigger Kit

Kit Contains:

1 Kenalog-40® (1mL)

1 Lidocaine HCl Injection, USP 1%

1 Ammonia Inhalant Ampule (35% Alcohol/15% Ammonia)

1 Povidone-Iodine Prep Pad

1 Pair Nitrile Powder Free Sterile Gloves* (M)

1 Drape

1 dhesive Bandage
Needles and Syringes Not Included
Distributed by
Enovachem™
PHARMACEUTICALS
Torrance, CA 90501
PHYSICIAN EZ USE JOINT TUNNEL AND TRIGGER KIT 
ammonia, lidocaine hydrochloride, triamcinolone acetonide, povidone-iodine kit
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:76420-524
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76420-524-01 1 in 1 CARTON; Type 1: Convenience Kit of Co-Package  
Quantity of Parts
Part # Package Quantity Total Product Quantity
Part 1 1 AMPULE  2 mL
Part 2 1 VIAL, SINGLE-DOSE  1 mL
Part 3 1 AMPULE  0.3 mL
Part 4 1 PACKET  2.2 g
Part 1 of 4
LIDOCAINE HYDROCHLORIDE 
lidocaine hydrochloride injection, solution
Product Information
Item Code (Source) NDC:0409-4713
Route of Administration INFILTRATION
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)  LIDOCAINE HYDROCHLORIDE ANHYDROUS 10 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  7 mg  in 1 mL
WATER (UNII: 059QF0KO0R)   
SODIUM HYDROXIDE (UNII: 55X04QC32I)   
HYDROCHLORIC ACID (UNII: QTT17582CB)   
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0409-4713-32 2 mL in 1 AMPULE; Type 0: Not a Combination Product  
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA080408 03/30/2010 
Part 2 of 4
KENALOG-40 
triamcino