FDA.reportPublic FDA data

Numbing Cream

Manufacturer
Everyday Medical LLC
Effective date
2019-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:18:51

Label at a glance#

ProductNumbing Cream
Active ingredientLIDOCAINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Lidocaine 5% Topical Analgesic

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

temporarily relieves minor pain associated with

  • arthritis
  • simple backache
  • muscle strains
  • bruises
  • sprains
  • cramps

WARNINGS SECTION

Warnings

For external use only

When using this product: Use only as directed

  • do not bandage tightly or use with a heating pad
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds or damaged, broken or irritated skin
  • if severe burning sensation occurs, discontinue use immediately

Stop use and ask a doctor if

  • condition worsens
  • redness is present
  • irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away​

DOSAGE & ADMINISTRATION SECTION

  • Use only as directed
  • Adults and children 12 years of age and older apply a thin layer to affected area every 6 to 8 hours not to exceed 3 applications in a 24 times period
  • Children under the age of 12 years of age consult a doctor

INACTIVE INGREDIENT SECTION

MELALEUCA ALTERNIFOLIA LEAF
CYCLOMETHICONE 5
PHENYL TRIMETHICONE
ALKYL (C12-15) BENZOATE
CLOVE OIL
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
WATER
ALOE VERA LEAF
CETYL ALCOHOL
LICORICE
GLYCERIN
STEARIC ACID
EDETIC ACID
GLYCERYL STEARATE/PEG-100 STEARATE
SODIUM HYDROXIDE
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE
BUTYLATED HYDROXYTOLUENE
CETOSTEARYL ALCOHOL
CETEARYL GLUCOSIDE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

numbing creamnumbing cream

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72982-190472982-1904-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CLOVE OIL578389D6D0IACT
LIDOCAINE98PI200987ACTIB
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CETYL ALCOHOL936JST6JCNIACT
LICORICE61ZBX54883IACT
GLYCERINPDC6A3C0OXIACT
STEARIC ACID4ELV7Z65APIACT
EDETIC ACID9G34HU7RV0IACT
GLYCERYL STEARATE/PEG-100 STEARATERD25J5V947IACT
SODIUM HYDROXIDE55X04QC32IIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT

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
b726c9ed-eeae-2473-e053-2995a90aed458d7db6c2-57fa-6b4d-e053-2995a90a31d82020-12-23WarningsExact identifier
spl set id: 8d7db6c2-57fa-6b4d-e053-2995a90a31d8

Reported adverse events (FAERS/openFDA)#

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