Label: PAIN RELIEF CREAM- lidocream hydrochloride cream
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Contains inactivated NDC Code(s)
NDC Code(s): 86089-222-01 - Packager: AEC Consumer Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 January 5, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Warning
- When using this product
- Stop use and ask a doctor if
- Keep out of use of children
- Storage and Handling
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Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aqua, Arnica Mountain Flower Extract, Astaxanthin, Benzyl Alcohol, BHT, Bisabolol, Boswellia Serrata Resin Extract, Cannabis Sativa Oil/Extract, Cetyl Alcohol, Citrus Aurantium Bergamia Peel Oil, Curcurria Longa Root Extract, Cyclopentasiloxane, Dimethicone, Dimethicol, Emu Oil, Ethoxydiglycol, Glucosamine, Glycerin, Glyceryl Stearate SE, Isopropyl Palmitate, Melaleuca Alternifolia Leaf Oil, Methylsulfonylmethane, PEG-100 Stearate, Phenoxyethanol, Polyquaterium-10, Potassium Sorbate, Propylene Glycol, Retinyl Palmitate, Salicylic Acid, Sodium Hydroxide, Stearic Acid, Stearyl Alcohol, Tetrasodium EDTA, Tocopherol, Triethanolamine, Vaccinium Myrtillus Fruit/Leaf Extract
- Indications
- Do not use
- Ask a doctor
- Directions
- dosage
- image of label
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INGREDIENTS AND APPEARANCE
PAIN RELIEF CREAM
lidocream hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:86089-222 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 3.86 g in 100 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) water (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASTAXANTHIN (UNII: 8XPW32PR7I) BENZYL ALCOHOL (UNII: LKG8494WBH) BISABOLOL OXIDE A (UNII: 16AE65F94Y) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) CETYL ALCOHOL (UNII: 936JST6JCN) CITRUS AURANTIIFOLIA FRUIT OIL (UNII: 7937R189CB) CURCUMA LONGA LEAF (UNII: H2HC4RY52C) DIMETHICONE (UNII: 92RU3N3Y1O) EMU OIL (UNII: 344821WD61) ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO) GLUCOSAMINE (UNII: N08U5BOQ1K) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TETRASODIUM DIETHYLENETRIAMINEPENTAMETHYLENEPHOSPHONATE (UNII: E6DVO371LC) TOCOPHEROL (UNII: R0ZB2556P8) VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86089-222-01 94.6 g in 1 TUBE; Type 0: Not a Combination Product 09/23/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/23/2019 Labeler - AEC Consumer Products (080994102) Registrant - Cospro Development Corp (785638821) Establishment Name Address ID/FEI Business Operations Cospro Development Corp 785638821 manufacture(86089-222) , pack(86089-222) , label(86089-222)