Label: LIVCALM- aloe ferox leaf, activated charcoal, goldenseal, strychnos nux-vomica seed, okoubaka aubrevillei bark, and berberis vulgaris root bark solution/ drops
- NDC Code(s): 59469-328-40
- Packager: PEKANA Natuheilmittel GmbH
- 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 27, 2022
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- Indications
- Dosage
- Warning
- STORAGE AND HANDLING
- Tamper Evident
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box
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INGREDIENTS AND APPEARANCE
LIVCALM
aloe ferox leaf, activated charcoal, goldenseal, strychnos nux-vomica seed, okoubaka aubrevillei bark, and berberis vulgaris root bark solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59469-328 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALOE FEROX LEAF (UNII: 0D145J8EME) (ALOE FEROX LEAF - UNII:0D145J8EME) ALOE FEROX LEAF 6 [hp_X] in 100 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 6 [hp_X] in 100 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 6 [hp_X] in 100 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] in 100 mL OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (OKOUBAKA AUBREVILLEI BARK - UNII:MK2074187Z) OKOUBAKA AUBREVILLEI BARK 6 [hp_X] in 100 mL BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 12 [hp_X] in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59469-328-40 1 in 1 BOX 01/14/2020 1 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 01/14/2020 Labeler - PEKANA Natuheilmittel GmbH (320344542) Establishment Name Address ID/FEI Business Operations PEKANA Natuheilmittel GmbH 320344542 MANUFACTURE(59469-328)