Label: LIDOPRO PAIN RELIEF- capsaicin and lidocaine ointment
- NDC Code(s): 83881-001-35
- Packager: Clinic Pharma
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 19, 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 damaged, irritated or infected skin
- with a bandage or heating pad
- if you are allergic to any ingredients in this product
Stop use and ask doctor if
- condition worsens
- excessive skin
- irritation develops
- symptoms persist for more than 7 days
- symptoms clear up and occur again within 3 days
- Directions
- Other information
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Inactive ingredient
allantoin, aloe barbadensis leaf juice, ammonium acryloyldimethyltaurate/vp copolymer, cetyl alcohol, chamomilla recutita matricaria flower extract, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin, glyceryl stearate, inulin lauryl carbamate, PEG-100 stearate, phenoxyethanol, stearic acid, triethanolamine, water
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INGREDIENTS AND APPEARANCE
LIDOPRO PAIN RELIEF
capsaicin and lidocaine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83881-001 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL, (+)- - UNII:C6B1OE8P3W) MENTHOL, (+)- 10 mg in 100 mg LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 mg in 100 mg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 27.5 mg in 100 mg CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.0325 mg in 100 mg Inactive Ingredients Ingredient Name Strength ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X) TRIETHANOLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) GLYCERYL STEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PEG-100 STEARATE (UNII: YD01N1999R) ALLANTOIN (UNII: 344S277G0Z) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83881-001-35 1 in 1 BOX 11/19/2024 1 9900 mg in 1 TUBE, WITH APPLICATOR; 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 11/19/2024 Labeler - Clinic Pharma (119158469) Registrant - Clinic Pharma (119158469)