CVS LIDOCAINE PAIN RELIEF DRY- menthol, unspecified form, lidocaine spray 
Natural Essentials, Inc.

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.

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Drug Facts

Active ingredients

Lidocaine 4%

Menthol 1%

Purpose

Topical analgesic

Topical analgesic

Use

Warnings

For external use only

Flammable:

Do not use

  • 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

  • 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

  • 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,

  • ask a health professional before use.

Keep out of reach of children and pets.

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

Directions

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

Inactive ingredients

Alcohol Denatured, Caprylic/Capric Triglyceride, Propylene Glycol

Principal Display Panel – 113 g Can Label

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%

SPRAYS AT
ANY ANGLE

NET WT 4 0Z (113 g)

Figure
CVS LIDOCAINE PAIN RELIEF DRY 
menthol, unspecified form, lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-257
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM10 mg  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66902-257-04113 g in 1 CAN; Type 0: Not a Combination Product01/21/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/21/2021
Labeler - Natural Essentials, Inc. (947484713)
Establishment
NameAddressID/FEIBusiness Operations
NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-257)

Revised: 6/2023
Document Id: 3177f89a-af41-45e8-905e-91db6c1ff7b1
Set id: c20a4954-df80-4dce-9582-8b49e2a497bb
Version: 2
Effective Time: 20230612
 
Natural Essentials, Inc.