FDA.reportPublic FDA data

LIDOCAINE

Manufacturer
SUNFLORA, INC
Effective date
2022-05-24
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 22:00:35

Label at a glance#

ProductLIDOCAINE
Active ingredientLIDOCAINE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3oz3oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73240-004-032024-11-21C16284748780-11030e365-577d-111a-e063-dadaa90a10e273240-004-03
73240-004-032024-01-30C16284748780-11030e365-577d-111a-e063-dadaa90a10e273240-004-03

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73240-00473240-004-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
WATER059QF0KO0RIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIMETHICONE 1000MCU2324216IACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
ARNICA MONTANA FLOWER WATERU7L2JP51PRIACT
LIDOCAINE98PI200987ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
275e1aed-7991-7f26-e063-6394a90aa0f2b9cfcc8d-c3f4-d253-e053-2a95a90a31b32024-11-20Exact identifier
spl set id: b9cfcc8d-c3f4-d253-e053-2a95a90a31b3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.