Label: CHAVITA 7- aur met, calc sulf, cerebrum, hypericum perforatum, lachesis mutus, millefolium, valeriana liquid
- NDC Code(s): 66343-088-60
- Packager: RUBIMED AG
- 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 19, 2022
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ACTIVE INGREDIENT
Drug Facts Active Ingredients: (HPUS*) 14.3% of each
Aur met 200C Calc sulf 200C
Cerebrum 21X Hypericum perforatum 21X
Lachesis mutus 21X Millefolium 21X
Valeriana 21X*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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INGREDIENTS AND APPEARANCE
CHAVITA 7
aur met, calc sulf, cerebrum, hypericum perforatum, lachesis mutus, millefolium, valeriana liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-088 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 200 [hp_C] in 60 mL CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE ANHYDROUS 200 [hp_C] in 60 mL SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532) SUS SCROFA CEREBRUM 21 [hp_X] in 60 mL HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM WHOLE 21 [hp_X] in 60 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 21 [hp_X] in 60 mL ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK) ACHILLEA MILLEFOLIUM WHOLE 21 [hp_X] in 60 mL VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN 21 [hp_X] in 60 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66343-088-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/2022 Labeler - RUBIMED AG (480582035)
