Cocculus Indicus by Hahnemann Laboratories, INC. COCCULUS INDICUS pellet
Cocculus Indicus by
Drug Labeling and Warnings
Cocculus Indicus 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
COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0472 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0472-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0472-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0472-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0472-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0466 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0466-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0466-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0466-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0469 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0469-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0469-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0469-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0469-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0470 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0470-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0470-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0470-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0470-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0468 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0468-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0468-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0468-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0468-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0467 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0467-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0467-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0467-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0467-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0473 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0473-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0471 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0471-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0471-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0471-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 4 NDC: 37662-0471-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 COCCULUS INDICUS
cocculus indicus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0465 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 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: 37662-0465-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 2 NDC: 37662-0465-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 3 NDC: 37662-0465-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0465, 37662-0466, 37662-0467, 37662-0468, 37662-0469, 37662-0470, 37662-0471, 37662-0472, 37662-0473)
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.