Label: HEMPVANA ULTRA PAIN RELIEF - NERVE RELIEF- arnica montana, aconitum napellus, hypericum perforatum, ledum palustre, magnesia phosphorica, secale cornutum, silicea cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated April 12, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredients

    Arnica montana 12X HPUS

    Aconitum napellus 12X HPUS

    Hypericum perforatum 12X HPUS

    Ledum palustre 12X HPUS

    Magnesia phosphorica 12X HPUS

    Secale cornutum 12X HPUS

    Silicea 12X HPUS

  • Purpose

    Arnica montana 12X HPUS............................Pain

    Aconitum napellus 12X HPUS........................Numbness, Tingling, Shooting Pains

    Hypericum perforatum 12X HPUS..................Nerve Pain, Crawling Sensation

    Ledum palustre 12X HPUS.............................Joint Pain

    Magnesia phosphorica 12X HPUS..................Nerve Pain, Cramps

    Secale cornutum 12X HPUS...........................Pain, Tingling

    Silicea 12X HPUS............................................Pain in Toes and Fingers

  • Uses

    for the temporary relief of nerve pain

    Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA, and product has not been clinically tested.

  • 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.

    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 prsent 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

    • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
    • Children under 2 years of age: consult a physician.
  • Other information

    Store tightly closed in a cool dry place.

  • Inactive ingredients

    Water/Aqua/Eau, Ethylhexyl Stearate, Butylene Glycol, Stearic Acid, Dimethicone, Caprylic/Capric Trigylceride, PEG-100 Stearate, Glyceryl Stearate, Cannabis Sativa (Hemp) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Cetearyl Alcohol, Allantoin, Phenoxyethanol, Tocopheryl Acetate, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hexylene Glycol, Ethylhexylglycerin, Disodium EDTA, Sodium Hydroxide, Potassium Sorbate, Citric Acid, Red 4 (CI 14700), Blue 1 (CI 42090)

  • Questions?

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

  • PRINCIPAL DISPLAY PANEL

    Hempvana Brand

    NDC 73287-027-01

    Ultra Pain Relief Cream

    Nerve Relief

    + Hemp Seed Oil

    For Moisturization

    Homeopathic

    For the temporary relief of nerve pain

    Net Wt. 3 OZ (85 g)

    1

    2

  • INGREDIENTS AND APPEARANCE
    HEMPVANA ULTRA PAIN RELIEF - NERVE RELIEF 
    arnica montana, aconitum napellus, hypericum perforatum, ledum palustre, magnesia phosphorica, secale cornutum, silicea cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73287-027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS12 [hp_X]  in 85 g
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA12 [hp_X]  in 85 g
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM12 [hp_X]  in 85 g
    LEDUM PALUSTRE WHOLE (UNII: 1N8KG72C5M) (LEDUM PALUSTRE WHOLE - UNII:1N8KG72C5M) LEDUM PALUSTRE WHOLE12 [hp_X]  in 85 g
    CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (CLAVICEPS PURPUREA SCLEROTIUM - UNII:01G9XEA93N) CLAVICEPS PURPUREA SCLEROTIUM12 [hp_X]  in 85 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 85 g
    MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE12 [hp_X]  in 85 g
    Inactive Ingredients
    Ingredient NameStrength
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73287-027-011 in 1 CARTON04/12/2023
    185 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/12/2023
    Labeler - TELEBRANDS CORP (177266558)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neutraderm, Inc.146224444manufacture(73287-027)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!