Label: CHAVITA 4- aur met, crataegus, cetraria, eucalyptus globulus, ferrum met, thymus gland, zinc val liquid
- NDC Code(s): 66343-085-60
- 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 21X Crataegus 21X
Cetraria 21X Eucalyptus globulus 21X
Ferrum met 50C Thymus gland 21X
Zinc val 200C*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 4
aur met, crataegus, cetraria, eucalyptus globulus, ferrum met, thymus gland, zinc val liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-085 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 21 [hp_X] in 60 mL HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36) HAWTHORN LEAF WITH FLOWER 21 [hp_X] in 60 mL CETRARIA ISLANDICA WHOLE (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA WHOLE - UNII:BJ7YPN79A1) CETRARIA ISLANDICA WHOLE 21 [hp_X] in 60 mL EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 21 [hp_X] in 60 mL IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 50 [hp_C] in 60 mL BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (BOS TAURUS THYMUS - UNII:8XEJ88V2T8) BOS TAURUS THYMUS 21 [hp_X] in 60 mL ZINC VALERATE DIHYDRATE (UNII: MN0RX54EQA) (VALERIC ACID - UNII:GZK92PJM7B) ZINC VALERATE DIHYDRATE 200 [hp_C] 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:66343-085-60 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)
