Label: CAND-EX- lycopodium,nux vomica,borax,asafoetida,nux moschata,gentiana lutea,kreosotum,calcarea carbonica,sepia,phosphoric acid,echinacea,pulsatilla,baptisia, liquid

  • NDC Code(s): 61657-0101-1
  • Packager: WHITE MANUFACTURING INC. DBA MICRO WEST
  • Category: HUMAN OTC DRUG LABEL

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 January 21, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENTS

    Asafoetida 12X

    Baptisia 3X

    Borax 12X

    Calc carb 12X

    Echinacea 3X

    Gentiana lut 3X

    Kreosotum 12X

    Lycopodium 30X

    Nux mosch 12X

    Nux vom 12X

    Phosphoricum ac 12X

    Pulsatilla 30X

    Sepia 30X

  • Inactive ingredients

    Inactive ingredients: Alcohol (20% v/v), Purified water

  • PURPOSE

    FOR THE TEMPORARY RELIEF OF FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS

    INDICATIONS: FOR THE TEMPORARY RELIEF OF FLATULENCE, DROWSINESS, CONFUSION, VERITGO, HEADACHE, NAUSEA, AND VAGINAL DISCHARGE

  • WARNING

    WARNINGS: Stop use and call a doctor if symptoms persist or worsen. If pregnant or breast-feeding, consult a healthcare professional before use. Contains alcohol; in case of accidental overdose, consult a poison control center immediately.

  • DIRECTIONS

    DIRECTIONS:Take 6 drops orally, 4 times a day. For ages 2 to adult

  • Other Information

    Other information: Tamper resistant for your protection. Use only if safety seal is intact

  • MANUFACTURE

    MANUFACTURED FOR:

    MICRO WEST

    P.O. Box 950

    DOUGLAS, WY 82633
    1-307-358-5066

  • LABEL

    NDC 61657-0101-1

    MICRO-WEST

    Homeopathic

    CAND-EX

    Product #: 0101

    1.0 fl oz Bottle Label

    1.0  fl oz (29.6 mL)

    Ethanol 20%

  • INGREDIENTS AND APPEARANCE
    CAND-EX 
    lycopodium,nux vomica,borax,asafoetida,nux moschata,gentiana lutea,kreosotum,calcarea carbonica,sepia,phosphoric acid,echinacea,pulsatilla,baptisia, liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61657-0101
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE30 [hp_X]  in 30 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED12 [hp_X]  in 30 mL
    ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED3 [hp_X]  in 30 mL
    BAPTISIA TINCTORIA (UNII: 5K1UO2888Y) (BAPTISIA TINCTORIA - UNII:5K1UO2888Y) BAPTISIA TINCTORIA3 [hp_X]  in 30 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS30 [hp_X]  in 30 mL
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE30 [hp_X]  in 30 mL
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID12 [hp_X]  in 30 mL
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE12 [hp_X]  in 30 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]  in 30 mL
    SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE12 [hp_X]  in 30 mL
    GENTIANA LUTEA ROOT (UNII: S72O3284MS) (GENTIANA LUTEA ROOT - UNII:S72O3284MS) GENTIANA LUTEA ROOT3 [hp_X]  in 30 mL
    NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG12 [hp_X]  in 30 mL
    ASAFETIDA (UNII: W9FZA51AS1) (ASAFETIDA - UNII:W9FZA51AS1) ASAFETIDA12 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61657-0101-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/01/1993
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/01/1993
    Labeler - WHITE MANUFACTURING INC. DBA MICRO WEST (082307831)