FDA.reportPublic FDA data

CVS Lidocaine Pain Relief Dry

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 20:53:44

Label at a glance#

ProductCVS Lidocaine Pain Relief Dry
Active ingredientMENTHOL, UNSPECIFIED FORM, LIDOCAINE
Label structure7 sections

Dosage and administration

shake well adults and children 12 years of age and older: spray product on area not more than 1 to 3 times daily product will dry quickly on its own, and does not need to be rubbed in children under 12 years of age or younger: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

  • temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Flammable:

  • do not use while smoking or near heat or flame
  • avoid long term storage above 104°F (40°C)
  • do not store at temperatures above 120°F(49°C)

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • rare cases of serious burns have been reported with products of this type
  • do not allow contact with eyes or mucous membranes
  • avoid spraying on face
  • avoid inhalation of spray
  • do not bandage tightly
  • do not use with a heating pad or other topical pain relief products
  • contents under pressure
  • do not puncture or incinerate.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • needed for longer than a week

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

  • shake well
  • adults and children 12 years of age and older:
  • spray product on area not more than 1 to 3 times daily
  • product will dry quickly on its own, and does not need to be rubbed in

children under 12 years of age or younger:ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denatured, Caprylic/Capric Triglyceride, Propylene Glycol

Principal Display Panel – 113 g Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS
Health ®

Compare to active
ingredients in IcyHot ®
Lidocaine Dry Spray*

MAXIMUM STRENGTH

Lidocaine concentration
without a prescription ✝

Lidocaine
Pain Relief
Dry Spray

PLUS MENTHOL

LIDOCAINE 4%
MENTHOL 1%

  • Desensitizes aggravated
    nerves
  • Dries instantly
  • Fast & long-lasting relief
  • No-mess continuous
    spray

SPRAYS AT
ANY ANGLE

NET WT 4 0Z (113 g)

Figure
Figure

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66902-257CVS LIDOCAINE PAIN RELIEF DRY (MENTHOL, UNSPECIFIED FORM, LIDOCAINE) SPRAY [NATURAL ESSENTIALS, INC.]3Legacy NDC20241004_c20a4954-df80-4dce-9582-8b49e2a497bb.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66902-25766902-257-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
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
2398deab-520a-61d4-e063-6394a90a3fd8c20a4954-df80-4dce-9582-8b49e2a497bb2024-10-03WarningsExact identifier
spl id: 2398deab-520a-61d4-e063-6394a90a3fd8
spl set id: c20a4954-df80-4dce-9582-8b49e2a497bb

Reported adverse events (FAERS/openFDA)#

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