PULSATILLA NIGRICANS pellet
Pulsatilla Nigricans by
Drug Labeling and Warnings
Pulsatilla Nigricans 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
PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4015 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4015-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4015-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4015-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4019 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4019-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4019-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4019-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4019-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4020 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4020-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4020-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4020-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4020-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4021 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4021-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4021-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4021-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4021-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4016 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4016-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4016-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4016-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4017 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4017-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4017-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4017-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4017-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4022 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4022-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4022-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4022-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4022-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4018 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4018-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 2 NDC: 37662-4018-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 09/25/2023 3 NDC: 37662-4018-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 4 NDC: 37662-4018-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 PULSATILLA NIGRICANS
pulsatilla nigricans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4023 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 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: 37662-4023-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-4015, 37662-4016, 37662-4017, 37662-4018, 37662-4019, 37662-4020, 37662-4021, 37662-4022, 37662-4023)
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