Label: HEMPVANA ULTRA STRENGTH PAIN RELIEF - OVERNIGHT- lidocaine cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 30, 2024

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  • Active Ingredient

    Lidocaine 4%

  • Purpose

    Lidocaine 4%...... Topical Analgesic

  • Uses

    For the temporary relief of pain

  • Warnings

    For external use only

    Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

    When using this product
    ■ use only as directed. Read and follow all directions and warnings on this label.
    ■ do not bandage tightly or apply local heat (such as heating pads) to the area
    of use.
    ■ avoid contact with eyes or mucous membranes.
    ■ do not apply to wounds or damaged, broken or irritated skin.
    ■ do not use at the same time as other topical analgesics.
    ■ do not use in large quantities, particularly over raw surfaces or blistered areas.

    Stop use and ask a doctor if
    ■ condition worsens
    ■ symptoms persist for more than 7 days or clear up and occur
    again within a few days
    ■ redness is present or irritation develops

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    ■ For Use By Adults Only
    ■ Apply generously to affected area
    ■ Massage into painful area until thoroughly absorbed into skin.
    ■ Repeat as necessary, but no more than 4 times daily.

  • Inactive Ingredients

    Water/Aqua/Eau, Propylene Glycol, Ethylhexyl Palmitate, Stearic Acid, Dimethicone, PEG-100 Stearate, Glyceryl Stearate, Cetearyl Alcohol, Hemp (Cannabis Sativa) Seed Oil, Lavender (Lavandula Angustifolia) Oil, Cocoa (Theobroma Cacao) Seed Butter, Lavender (Lavandula Angustifolia) Flower Extract, English/Roman Chamomile (Chamaemelum Nobile) Flower Extract, Melatonin, Kava (Piper Methysticum) Root Extract, Allantoin, Potassium Cetyl Phosphate, Glycerin, Tocopheryl Acetate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isohexadecane, Hexylene Glycol, Ethylhexylglycerin, Polysorbate 80, Disodium EDTA, Sodium Hydroxide, Red 4 (CI 14700), Blue 1 (CI 42090)

  • Questions

    Call (855) 877-4503 (M-F, 9am-5pm EST)

  • PRINCIPAL DISPLAY PANEL

    Hempvana

    Ultra Strength

    Pain Relief

    Cream

    Lidocaine 4%

    Overnight

    Lavender Scent

    Melatonin

    + Hemp Seed Oil

    For Moisturization

    Net Wt. 3oz (85 g)

    1

  • INGREDIENTS AND APPEARANCE
    HEMPVANA ULTRA STRENGTH PAIN RELIEF - OVERNIGHT 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73287-029
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    MELATONIN (UNII: JL5DK93RCL)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73287-029-011 in 1 CARTON01/30/2024
    185 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/30/2024
    Labeler - Telebrands Corp (177266558)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neutraderm, Inc.146224444manufacture(73287-029)
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