Label: ASPERCREME LIDOCAINE FOOT (DIABETIC)- lidocaine hydrochloride cream
- NDC Code(s): 41167-0597-0
- Packager: Chattem, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 23, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only
Do not use
■ if you have serious foot problems, such as ulcers or infections
■ if you have numbness or reduced ability to feel pain
■ 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 warning on this carton.
■ do not allow contact with the eyes and the mucous membranes
■ do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
■ do not use at the same time as other topical analgesics
- Directions
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Inactive ingredients
water, alcohol denat. (10%), cetearyl alcohol, ceteth-20 phosphate, dimethicone, caprylyl methicone, dicetyl phosphate, glyceryl stearate, aloe barbadensis leaf juice, panthenol, tocopheryl acetate, magnesium ascorbyl phosphate, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, methylparaben, disodium EDTA, citric acid
333-105
Child-resistant packaging. Close cap tightly after use.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ASPERCREME LIDOCAINE FOOT (DIABETIC)
lidocaine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0597 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETETH-20 PHOSPHATE (UNII: 921FTA1500) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) METHYLPARABEN (UNII: A2I8C7HI9T) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41167-0597-0 1 in 1 CARTON 06/01/2018 1 113 g in 1 BOTTLE, PLASTIC; 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 06/01/2018 Labeler - Chattem, Inc. (003336013)