Label: LIDOCAINE 2%- lidocaine injection
- NDC Code(s): 13985-222-04, 13985-222-05
- Packager: MWI/VetOne
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 14, 2020
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- INDICATIONS & USAGE
- CONTRAINDICATIONS
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PRECAUTIONS
Lidocaine is usually well tolerated. Nevertheless, as with all local anesthetics, untoward effects may occur due to hypersensitivity, faulty technique, overdosage and inadvertent intravascular or subarachnoid injection. In case of respiratory arrest, immediate resuscitation with oxygen is indicated.
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CONTAINS
Each mL of sterile aqueous solution contains:
Lidocaine Hydrochloride ............. 2.0%
Propylene Glycol ....................... 5.2%
Sodium Chloride ........................ 0.5%
Sodium Lactate ......................... 0.5%with Methylparaben 0.15%, Sodium Metabisulfite 0.10%,
Propylparaben 0.03%, Disodium Edetate 0.001% as preservatives.
- DOSAGE AND ADMINISTRATION
- STORAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIDOCAINE 2%
lidocaine injectionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:13985-222 Route of Administration EPIDURAL, INFILTRATION Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 0.02 g in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-222-04 100 mL in 1 BOTTLE 2 NDC:13985-222-05 250 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/02/2011 Labeler - MWI/VetOne (019926120)