Label: WALGREENS LIDOCAINE PLUS CREAM- benzyl alcohol and lidocaine hydrochloride cream
- NDC Code(s): 0363-9951-03
- Packager: Walgreens Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 9, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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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
alcohol 95%, aloe vera leaf, aminomethylpropanol, butylene glycol,carbomer interpolymer type A (allylsucrose crosslinked), ceteth-10
phosphate, cetostearyl alcohol, dihexadecyl phosphate, dimethicone,glyceryl 1-stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer (1001.5%), maltodextrin, polysorbate 80, steareth-21, water - Questions or comments?
- Package
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INGREDIENTS AND APPEARANCE
WALGREENS LIDOCAINE PLUS CREAM
benzyl alcohol and lidocaine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9951 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 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 40 mg in 1 g Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) MALTODEXTRIN (UNII: 7CVR7L4A2D) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) POLYSORBATE 80 (UNII: 6OZP39ZG8H) STEARETH-21 (UNII: 53J3F32P58) DEHYDRATED ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9951-03 1 in 1 BOX 02/01/2023 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 Drug M017 02/01/2023 Labeler - Walgreens Company (008965063) Establishment Name Address ID/FEI Business Operations Nantong Health & Beyond Hygienic Products Inc. 421280161 manufacture(0363-9951)