Label: DIGITALIS PURPUREA pellet
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NDC Code(s):
37662-0816-1,
37662-0816-2,
37662-0816-3,
37662-0817-1, view more37662-0817-2, 37662-0817-3, 37662-0818-1, 37662-0818-2, 37662-0818-3, 37662-0818-4, 37662-0819-1, 37662-0819-2, 37662-0819-3, 37662-0819-4, 37662-0820-1, 37662-0820-2, 37662-0820-3, 37662-0820-4, 37662-0821-1, 37662-0821-2, 37662-0821-3, 37662-0821-4, 37662-0822-1, 37662-0822-2, 37662-0822-3, 37662-0822-4, 37662-0823-1, 37662-0823-2, 37662-0823-3, 37662-0823-4, 37662-0824-1
- Packager: Hahnemann Laboratories, INC.
- 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 12, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0816 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0816-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0816-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0816-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0819 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0819-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0819-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0819-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0819-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0817 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0817-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0817-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0817-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0820 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0820-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0820-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0820-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0820-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0818 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0818-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0818-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0818-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0818-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0823 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0823-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0823-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0823-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0823-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0824 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0824-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0821 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0821-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0821-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0821-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0821-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 DIGITALIS PURPUREA
digitalis purpurea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0822 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS 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:37662-0822-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 2 NDC:37662-0822-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/12/2022 3 NDC:37662-0822-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 4 NDC:37662-0822-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0816, 37662-0817, 37662-0818, 37662-0819, 37662-0820, 37662-0821, 37662-0822, 37662-0823, 37662-0824)
