Rumex Crispus by Hahnemann Laboratories, INC. RUMEX CRISPUS pellet
Rumex Crispus by
Drug Labeling and Warnings
Rumex Crispus by is a Homeopathic medication manufactured, distributed, or labeled by Hahnemann Laboratories, INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2001-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2001-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2001-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 12 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2002-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2002-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2002-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 100 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2004-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2004-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2004-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2004-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2003 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2003-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2003-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2003-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2003-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2005 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2005-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2005-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2005-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2005-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 500 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2006-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2006-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2006-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2006-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2007 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2007-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2007-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2007-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2007-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2008 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 10 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2008-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 2 NDC: 37662-2008-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/22/2022 3 NDC: 37662-2008-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 4 NDC: 37662-2008-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 RUMEX CRISPUS
rumex crispus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 1 [hp_Q] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 1mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-2009-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/22/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2001, 37662-2002, 37662-2003, 37662-2004, 37662-2005, 37662-2006, 37662-2007, 37662-2008, 37662-2009)
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.