Label: CVS HEALTH LIDOCAINE PAIN RELIEF PLUS MENTHOL- lidocaine, menthol, unspecified form patch
- NDC Code(s): 66902-220-05
- Packager: Natural Essentials, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 19, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
-
Warnings
For external use only
Do not use
- more than 1 patch on your body at a time or on cut, irritated or swollen skin
- on puncture wounds
- for more than one week without consulting a doctor
When using this product
- use only as directed. Read and follow all directions and warnings on this carton.
- Do not use more than one patch in an 8 hour period. Maximum 3 patches per day.
- Rare cases of serious burns have been reported with products of this type
- Do not apply to wounds or damaged, broken or irritated skin
- Do not allow contact with the eyes and mucous membranes
- Do not bandage tightly or apply local heat (such as heating pads) to the area of use
- Do not use at the same time as other topical analgesics
- Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug products that can produce serious adverse effects if a child or pet chews or ingests this patch
- NOTE: patches may not adhere as well to all individuals, skin types, or certain parts of the body.
-
Directions
- Adults/children 12 years and older
- clean and dry affected area
- remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
- carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
- once exposed portion of patch is positioned, carefully remove remaining backing completely to apply patch to affected area
- once applied, press firmly and rub on all sides and center of patch to help adhesive adhere to skin
- do not remove patch and reapply, this will result in the patch not sticking
- avoid strenuous exercise while wearing patch, this will result in patch not sticking
- do not use more than one patch in an 8 hour period.
Children 12 years or younger: ask a doctor.
- Other information
- Inactive ingredients
-
Principal Display Panel – Box Label
CVS
Health®Compare to the active ingredients
in IcyHot® Lidocaine Patch
Plus Menthol*MAXIMUM STRENGTH
Lidocaine concentration without a prescription†
Lidocaine Pain
Relief PatchPLUS MENTHOL
LIDOCAINE 4%
MENTHOL 1%
-
Desensitizes
aggravated nerves - Easy to apply
- Fast acting
Topical Anesthetic
Topical Analgesic
Package Contains 5 Individually Wrapped Patches
5 PATCHES
3 15/16 IN X 5 1/2 IN (10 cm X 14 cm)
Pain-relieving ointment on a breathable adhesive pad
EACH PATCH IS SEALED IN A CHILD-RESISTANT POUCH FOR SAFETY
†Among over-the-counter
topical analgesics. -
Desensitizes
-
Principal Display Panel – Patch Label
CVS
Health®MAXIMUM STRENGTH
Lidocaine concentration without a prescription†
Lidocaine Pain
Relief PatchPLUS MENTHOL
LIDOCAINE 4%
MENTHOL 1%
-
Desensitizes
aggravated nerves - Easy to apply
- Fast acting
Topical Anesthetic
Topical Analgesic
1 PATCH
3 15/16 IN X 5 1/2 IN
(10 cm X 14 cm)†Among over-the-counter
topical analgesics. -
Desensitizes
-
INGREDIENTS AND APPEARANCE
CVS HEALTH LIDOCAINE PAIN RELIEF PLUS MENTHOL
lidocaine, menthol, unspecified form patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66902-220 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine 240 mg Menthol, unspecified form (UNII: L7T10EIP3A) (Menthol, unspecified form - UNII:L7T10EIP3A) Menthol, unspecified form 60 mg Inactive Ingredients Ingredient Name Strength DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) GLYCERIN (UNII: PDC6A3C0OX) KAOLIN (UNII: 24H4NWX5CO) METHYLPARABEN (UNII: A2I8C7HI9T) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) TARTARIC ACID (UNII: W4888I119H) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66902-220-05 5 in 1 BOX 12/18/2019 1 1 in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 12/18/2019 Labeler - Natural Essentials, Inc. (947484713) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co., Ltd. 529128763 MANUFACTURE(66902-220)