February 26, 2017
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Zingo

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Zingo

Indications
Dosage
How Supplied

INDICATIONS

ZINGO® is indicated for use on intact skin to provide topical local analgesia prior to venipuncture or peripheral intravenous cannulation, in children 3-18 years of age.

ZINGO® is indicated for use on intact skin to provide topical local analgesia prior to venipuncture in adults.

DOSAGE AND ADMINISTRATION

Apply one ZINGO® (0.5 mg lidocaine hydrochloride monohydrate) to the site planned for venipuncture or intravenous cannulation, one to three minutes prior to needle insertion. Perform the procedure within 10 minutes after ZINGO® administration.

Use ZINGO® only on intact skin.

Application of one additional ZINGO® at a new location is acceptable after a failed attempt at venous access. Multiple administration of ZINGO® at the same location are not recommended. When ZINGO® is used concomitantly with other products containing local anesthetic agents, the amount absorbed from all sources should be considered, as local anesthetics are thought to have at least additive toxicities.

Instructions For Use

Figure 1a And 1b

Prepare the treatment site and device - Illustration

Figure 2 ,3,4 and 5a

Injecting Zingo - Illustration

Figure 5b and 6

Using the safety feature - Illustration

Administering Zingo - Illustration

HOW SUPPLIED

Dosage Forms And Strengths

ZINGO® (lidocaine hydrochloride monohydrate) powder intradermal injection system contains 0.5mg of sterile lidocaine hydrochloride monohydrate.

Storage And Handling

NDC 70645-123-26 ZINGO® (lidocaine hydrochloride monohydrate) powder intradermal injection system contains 0.5mg of sterile lidocaine hydrochloride monohydrate. ZINGO® is a single-use device packaged in an individual clear pouch. Twelve pouched devices are placed in labeled cartons. Cartons are stored at controlled room temperature (15-30°C, 59-86°F).

Manufactured by: Powder Pharmaceuticals, Inc., Hong Kong, China. Distributed by: 7T Pharma LLC, Las Vegas, NV 89123, USA. Revised: May 2016

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 12/5/2016

Indications
Dosage
How Supplied

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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