Label: LIDOCAINE PLUS PAIN RELIEVING- lidocaine hydrochloride, benzyl alcohol liquid
- NDC Code(s): 51316-175-03
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 22, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
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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
- Directions
- Other information
- Inactive ingredients
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Principal Display Panel - 88 mL Carton Label
CVS
Health®
Compare to the active ingredients in Salonpas ® Lidocaine PLUS Liquid*
MAXIMUM STRENGTH
Lidociane concentration without a prescription †
Lidocaine Plus
Lidocaine HCl 4%
Benzyl Alcohol 10%
Topical anesthetics
Pain Relieving Liquid
- No-mess roll-on
- Fast-acting numbing relief
- Unscented
†Among over the counter topical analgesics
Actual Bottle Size on Side Panel
3 FL OZ (88 mL)

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INGREDIENTS AND APPEARANCE
LIDOCAINE PLUS PAIN RELIEVING
lidocaine hydrochloride, benzyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-175 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL 100 mg in 1 mL LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) CITRIC ACID (UNII: 2968PHW8QP) TROMETHAMINE (UNII: 023C2WHX2V) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-175-03 1 in 1 CARTON 02/02/2026 1 88 mL in 1 BOTTLE; 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 02/02/2026 Labeler - CVS Pharmacy (062312574) Registrant - Natural Essentials, Inc. (947484713) Establishment Name Address ID/FEI Business Operations Natural Essentials, Inc. 947484713 manufacture(51316-175)
