Label: LIDOCAINE liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73240-004-03 - Packager: SUNFLORA, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 24, 2022
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
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- ACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
LIDOCAINE
lidocaine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73240-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HEXYLENE GLYCOL (UNII: KEH0A3F75J) WATER (UNII: 059QF0KO0R) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONE 1000 (UNII: MCU2324216) XANTHAN GUM (UNII: TTV12P4NEE) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73240-004-03 85 g in 1 APPLICATOR; Type 0: Not a Combination Product 01/26/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/26/2021 Labeler - SUNFLORA, INC (067153368)
