FDA.reportPublic FDA data

Lidocaine Pain Relief with Lavender

Manufacturer
Natural Essentials, Inc.
Effective date
2024-10-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:53:45

Label at a glance#

ProductLidocaine Pain Relief with Lavender
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure9 sections

Dosage and administration

adults and children 12 years of age and over: apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period children 12 years or younger: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Use

INDICATIONS & USAGE SECTION

  • For the temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on large areas of the body or on cut, irritated or swollen skin
  • on puncture wounds
  • for more than one week without consulting a doctor

When using this product

OTC - WHEN USING SECTION

  • use only as directed. Read and follow all directions and warnings on this carton
  • do not allow contact with the eyes
  • do not bandage or apply local heat (such as heating pads) to area of use

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • conditions worsen
  • skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
  • symptoms persist for more than 7 days
  • symptoms dear up and occur again within a few days

Flammable: Keep away from fire or flame

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and over:
  • apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

children 12 years or younger:ask a doctor

Other information

OTHER SAFETY INFORMATION

  • Avoid storing product in direct sunlight
  • Protect product from excessive moisture
  • Store with lid closed tightly

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Acrylate Crosspolymer, Alcohol Denatured, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Caprylyl Methicone, Cetearyl Alcohol, Ceteth-20 Phosphate, Dicetyl Phosphate, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glyceryl Stearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Lavandula Angustifolia (Lavender) Oil, Methylparaben, Polysorbate 60, Steareth-2, Steareth-21, Water

Principal Display Panel – 73 mL Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS
Health ®

Compare to the active
ingredient in Aspercreme ®
Lidocaine with Lavender
Essential Oil*

MAXIMUM STRENGTH
Lidocaine concentration
without a prescription †

Lidocaine
Pain Relief
Roll-On

LIDOCAINE HCI 4%

Lavender Essential Oil

  • Temporary relief of pain
  • Helps numb pain-affected
    areas without irritation
  • Non-greasy, no-mess formula

With calming
lavender
aromatherapy

Actual Bottle
Size on
Side Panel

2.5 FL OZ
(73 mL)

Principal Display Panel – 73 mL Carton Label
Principal Display Panel – 73 mL Carton Label

Principal Display Panel – 73 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS
Health ®

MAXIMUM STRENGTH
Lidocaine concentration
without a prescription †

Lidocaine Pain
Relief Roll-On

LIDOCAINE HCI 4%

Lavender Essential Oil

With calming
lavender
aromatherapy

2.5 FL OZ (73 mL)

Principal Display Panel – 73 mL Bottle Label
Principal Display Panel – 73 mL Bottle Label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66902-057LIDOCAINE PAIN RELIEF WITH LAVENDER (LIDOCAINE HYDROCHLORIDE) LIQUID [NATURAL ESSENTIALS, INC.]3Legacy NDC20241004_ea1c78b3-7ae2-47b4-b45a-0c7fc623e592.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66902-05766902-057-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
ALCOHOL3K9958V90MIACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETETH-20 PHOSPHATE921FTA1500IACT
DIHEXADECYL PHOSPHATE2V6E5WN99NIACT
DIMETHICONE92RU3N3Y1OIACT
EDETATE DISODIUM7FLD91C86KIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)86FQE96TZ4IACT
ISOHEXADECANE918X1OUF1EIACT
LAVENDER OILZBP1YXW0H8IACT
METHYLPARABENA2I8C7HI9TIACT
POLYSORBATE 60CAL22UVI4MIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
WATER059QF0KO0RIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR

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
2398c2ec-985e-6198-e063-6394a90ad8efea1c78b3-7ae2-47b4-b45a-0c7fc623e5922024-10-03WarningsExact identifier
spl id: 2398c2ec-985e-6198-e063-6394a90ad8ef
spl set id: ea1c78b3-7ae2-47b4-b45a-0c7fc623e592

Reported adverse events (FAERS/openFDA)#

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