Label: CVS HEALTH LIDOCAINE PLUS PAIN RELIEVING- lidocaine hydrochloride, benzyl alcohol cream
- NDC Code(s): 66902-758-03
- Packager: NATURAL ESSENTIALS, INC.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated June 7, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
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Warnings
For external use only
Do not use
- on wounds or damaged skin
- in large 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
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Inactive ingredients
Acrylates/C10-30 Acrylate Crosspolymer, Aloe Vera Gel 10 X, Aminomethyl Propanol, Cetearyl Alcohol, Ceteth-20 Phosphate, Dicetyl Phosphate, Citric Acid, Deionized Water, Dimethicone, Hydroxyethyl Acrlyate/Sodium, Acryloyldimethyl Taurate Copolymer, Squalane, Polysorbate 60, Propylene Gylcol, SDA 40-B Alcohol, Steareth-21.
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Principal-Display Panel – 85 g Carton Label
CVS
Health™Compare to the
active ingredients in
Salonpas® Lidocaine
PLUS Cream*MAXIMUM STRENGTH
Lidocaine concentration
without a prescription✝Lidocaine
PlusPAIN RELIEVING CREAM
LIDOCAINE HCl 4%
BENZYL ALCOHOL 10%
Topical anesthetics
Non-greasy
- Fast acting
- Numbing relief
- Unscented
Non-greasy
creamPackage Contains
One Tube✝Among over the counter
topical analgesics.NET WT 3 0Z (85 g)
- Principal-Display Panel – 85 g Carton Label
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INGREDIENTS AND APPEARANCE
CVS HEALTH LIDOCAINE PLUS PAIN RELIEVING
lidocaine hydrochloride, benzyl alcohol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66902-758 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine Hydrochloride (UNII: V13007Z41A) (Lidocaine - UNII:98PI200987) Lidocaine Hydrochloride Anhydrous 40 mg in 1 g Benzyl Alcohol (UNII: LKG8494WBH) (Benzyl Alcohol - UNII:LKG8494WBH) Benzyl Alcohol 100 mg in 1 g Inactive Ingredients Ingredient Name Strength CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) ALOE VERA LEAF (UNII: ZY81Z83H0X) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETETH-20 PHOSPHATE (UNII: 921FTA1500) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) SQUALENE (UNII: 7QWM220FJH) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) STEARETH-21 (UNII: 53J3F32P58) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66902-758-03 1 in 1 BOX 04/23/2021 1 85 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/23/2021 Labeler - NATURAL ESSENTIALS, INC. (947484713) Establishment Name Address ID/FEI Business Operations NATURAL ESSENTIALS, INC. 947484713 MANUFACTURE(66902-758)