Label: EHA- lidocaine hydrochloride lotion
- NDC Code(s): 76420-351-30
- Packager: Asclemed USA, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated November 1, 2018
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- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warning
- Directions
- Inactive ingredients
- Principal Display Panel - 88 mL Bottle Label
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INGREDIENTS AND APPEARANCE
EHA
lidocaine hydrochloride lotionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:76420-351 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) LAURETH-7 (UNII: Z95S6G8201) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76420-351-30 88 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/07/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/07/2016 Labeler - Asclemed USA, Inc. (059888437)