Label: CHAVITA 5- phosphorus, thuja occidentalis, thyroidinum, viola tric liquid
- NDC Code(s): 66343-086-60
- 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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENT
Drug Facts Active Ingredients: (HPUS*) 25% of each
Phosphorus 21X
Thuja occidentalis 50C
Thyroidinum 21X
Viola tric 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.
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CHAVITA 5
phosphorus, thuja occidentalis, thyroidinum, viola tric liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-086 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 21 [hp_X] in 60 mL THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 50 [hp_C] in 60 mL THYROID, PORCINE (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) THYROID, PORCINE 21 [hp_X] in 60 mL VIOLA TRICOLOR WHOLE (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V) VIOLA TRICOLOR WHOLE 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:66343-086-60 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)
