Label: HANGOVER RELIEF- asafetida,capsicum,potassium dichromate,cola nut,lachesis muta venom,strychnos nux-vomica seed,ranunculus bulbosus,sulfuric acid,zinc. pellet

  • NDC Code(s): 61727-330-21
  • Packager: Homeocare Laboratories
  • 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 December 18, 2018

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  • Active ingredients:(HPUS)

    Asafoetida 5C, Capsicum annuum 5C, Kali bichromium 5C, Kola 5C, Lachesis mutus 5C, Nux vomica 5C, Ranuculus Bulbosa 7C, Sulphuricum acidum 5C, Zincum met. 5C.

  • Purpose:

    For the temporary relief of headache, nausea and vomiting associated with alcohol consumption.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Uses:

    For the temporary relief of headache, nausea and vomiting associated with alcohol consumption.

  • Warnings:

    If symptoms persist or worsen or if pregnant or nursing consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

  • Inactive ingredients:


    Sucrose/lactose.

  • Dosage & Administration:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue. 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

  • Hangover Relief

    Hangover Relief

    Homeopathic Medicine

    85 Pellets
    hangover relief image
    hcl_label_Hangover-2012.jpg


  • INGREDIENTS AND APPEARANCE
    HANGOVER RELIEF 
    asafetida,capsicum,potassium dichromate,cola nut,lachesis muta venom,strychnos nux-vomica seed,ranunculus bulbosus,sulfuric acid,zinc. pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-330
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASAFETIDA (UNII: W9FZA51AS1) (ASAFETIDA - UNII:W9FZA51AS1) ASAFETIDA5 [hp_C]  in 4 g
    CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM5 [hp_C]  in 4 g
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE5 [hp_C]  in 4 g
    COLA NUT (UNII: PQM9SA369U) (COLA NUT - UNII:PQM9SA369U) COLA NUT5 [hp_C]  in 4 g
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM5 [hp_C]  in 4 g
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED5 [hp_C]  in 4 g
    RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS7 [hp_C]  in 4 g
    SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID5 [hp_C]  in 4 g
    ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC5 [hp_C]  in 4 g
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-330-214 g in 1 TUBE; Type 0: Not a Combination Product11/23/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/23/2011
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-330)
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