Label: D-112- lachesis muta venom, silicon dioxide, sodium chloride, ranunculus bulbosus, aconitum napellus, activated charcoal, nitroglycerin, oyster shell calcium carbonate, crude, anemone pratensis, plantago major, arsenic trioxide, and magnesium phosphate, dibasic trihydrate solution

  • 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 July 12, 2018

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

  • SPL UNCLASSIFIED SECTION

    NDC 58264-0118-1

  • INDICATIONS

    Teeth sensitive to cold and heat.

  • INGREDIENTS

    ACTIVE

    Lachesis 12x, 30x, Silicea 8x, 30x, Natrum muriaticum 4x, 30x, Ranunculus bulbosus 4x, 12x, Aconitum napellus 4x, 15x, Carbo vegetabilis 8x, 12x, Glonoinum 6x, 30x, Calcarea carbonica 8x, 30x, Pulsatilla nigricans 4x, 30x, Plantago major 4x, 12x, Arsenicum album 6x, 30x, Magnesia phosphoricum 4x, 12x

    INACTIVE

    20% alcohol in purified water.

  • SUGGESTED DOSAGE

    One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

  • STORAGE AND HANDLING

    SHAKE WELL

  • Warnings

    • Use only if cap seal is unbroken.

    • If pregnant or breastfeeding, ask a healthcare professional before use.

    • Keep this and all medication out of the reach of children.
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

  • PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL

    ASSOCIATES, INC.

    D 112

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    D-112 
    lachesis muta venom, silicon dioxide, sodium chloride, ranunculus bulbosus, aconitum napellus, activated charcoal, nitroglycerin, oyster shell calcium carbonate, crude, anemone pratensis, plantago major, arsenic trioxide, and magnesium phosphate, dibasic trihydrate solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0118
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lachesis Muta venom (UNII: VSW71SS07I) (Lachesis Muta venom - UNII:VSW71SS07I) Lachesis Muta venom12 [hp_X]  in 1 mL
    Silicon dioxide (UNII: ETJ7Z6XBU4) (Silicon dioxide - UNII:ETJ7Z6XBU4) Silicon dioxide8 [hp_X]  in 1 mL
    Sodium chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) Sodium chloride4 [hp_X]  in 1 mL
    Ranunculus bulbosus (UNII: AEQ8NXJ0MB) (Ranunculus bulbosus - UNII:AEQ8NXJ0MB) Ranunculus bulbosus4 [hp_X]  in 1 mL
    Aconitum napellus (UNII: U0NQ8555JD) (Aconitum napellus - UNII:U0NQ8555JD) Aconitum napellus4 [hp_X]  in 1 mL
    Activated charcoal (UNII: 2P3VWU3H10) (Activated charcoal - UNII:2P3VWU3H10) Activated charcoal8 [hp_X]  in 1 mL
    Nitroglycerin (UNII: G59M7S0WS3) (Nitroglycerin - UNII:G59M7S0WS3) Nitroglycerin6 [hp_X]  in 1 mL
    Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I) Oyster shell calcium carbonate, crude8 [hp_X]  in 1 mL
    Anemone pratensis (UNII: 8E272251DI) (Anemone pratensis - UNII:8E272251DI) Anemone pratensis4 [hp_X]  in 1 mL
    Plantago major (UNII: W2469WNO6U) (Plantago major - UNII:W2469WNO6U) Plantago major4 [hp_X]  in 1 mL
    arsenic trioxide (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) arsenic trioxide6 [hp_X]  in 1 mL
    Magnesium phosphate, dibasic trihydrate (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) Magnesium phosphate, dibasic trihydrate4 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0118-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC01/01/1990
    Labeler - DNA Labs, Inc. (031784339)