Lidocaine Plus Pain Relieving
- Dosage form
- LIQUID
- Labeler
- CVS Pharmacy
- Label updated
- 2026-07-24
- Retrieved
- 2026-09-07
- Active ingredients
- BENZYL ALCOHOL
Active ingredients
Benzyl alcohol 10%
Lidocaine HCl 4%
Purpose
Topical anesthetic
Topical anesthetic
Use
For the temporary relief of pain
Warnings
For external use only.
Flammable: Keep away from fire or flame
Do not use
- on wounds or damaged skin
- in largge quantities
- with a heating pad
- if you are allergic to any ingredients of this product
When using this product
- use only as directed
- avoid contact with the eyes, mucous membranes or rashes
- do not bandage tightly
Stop use and ask a doctor if
- skin reactions occur, such as rash, itching, redness, irritatin, pain, swelling and blistering
- conditions worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
If pregnant or breast-feeding,
ask a health professional before use.
Keep ot of reach of children and pets.
If swallowed, get medical help or contactg a Poison Control Center right away.
Directions
- Adults and children 12 years of age and over:
- clean and dry affected area
- apply to affected area not more than 3 to 4 times daily
- Children under 12 years of age: ask a doctor
Other information
- Avoid storing product in direct sunlight
- Protect product from excessive moisture
- Store with lid closed tightly
Inactive ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Citric Acid, SD Alcohol 40-B, Tromethamine, Water
Principal Display Panel - 88 mL Carton Label
CVS TM
Maximum OTC Strength †
PAIN-
RELIEVING
ROLL-ON
Lidocaine Plus
Lidocaine HCl 4%
Benzyl Alcohol 10%
Compare to Salonpas ®
Lidocaine PLUS Liquid
active ingredients*
Two Powerful Topical
Anesthetics
Fast-Acting, Numbing Relief
No-Mess Roll-On
Fragrance Free
3 FL OZ (88 mL)
†Lidocaine concentration without a prescription.
Among over-the-counter topical analgesics
[Image in the official label — see DailyMed source]
DailyMed Set ID: 49003aac-184c-ae33-e063-6294a90a29c0 · Version 2
NDC: 51316-175