Label: CHAVITA 2- platinum, causticum, silver cyanide, thuja occidentalis leafy twig, juniper berry, lavandula angustifolia whole, and sus scrofa adrenal gland liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66343-007-50 - 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 July 6, 2015
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- PURPOSE
- Ingredients
- TAMPER-EVIDENT
- Direction
- Warnings
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label
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INGREDIENTS AND APPEARANCE
CHAVITA 2
platinum, causticum, silver cyanide, thuja occidentalis leafy twig, juniper berry, lavandula angustifolia whole, and sus scrofa adrenal gland liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-007 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLATINUM (UNII: 49DFR088MY) (PLATINUM - UNII:49DFR088MY) PLATINUM 50 [hp_C] in 1 mL CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 200 [hp_C] in 1 mL SILVER CYANIDE (UNII: 33RV6XQ01M) (SILVER CYANIDE - UNII:33RV6XQ01M) SILVER CYANIDE 21 [hp_X] in 1 mL THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 21 [hp_X] in 1 mL JUNIPER BERRY (UNII: O84B5194RL) (JUNIPER BERRY - UNII:O84B5194RL) JUNIPER BERRY 21 [hp_X] in 1 mL LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L) (LAVANDULA ANGUSTIFOLIA WHOLE - UNII:51217XIL5L) LAVANDULA ANGUSTIFOLIA WHOLE 21 [hp_X] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 21 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) 0.51 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66343-007-50 50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 05/07/2015 Labeler - RUBIMED AG (480582035) Establishment Name Address ID/FEI Business Operations RUBIMED AG 480582035 MANUFACTURE(66343-007) Establishment Name Address ID/FEI Business Operations Omida AG 483268348 MANUFACTURE(66343-007)
