XEROPHYLLUM ASPHODELOIDES pellet
Xerophyllum Asphodeloides by
Drug Labeling and Warnings
Xerophyllum Asphodeloides 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
XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2397 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2397-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2397-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2397-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2399 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2399-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2399-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2399-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 4 NDC: 37662-2399-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2398 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2398-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2398-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2398-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2400 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2400-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2400-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2400-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 4 NDC: 37662-2400-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2402 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2402-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2402-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2402-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 4 NDC: 37662-2402-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2403 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2403-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2403-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2403-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 4 NDC: 37662-2403-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 XEROPHYLLUM ASPHODELOIDES
xerophyllum asphodeloides pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-2401 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES 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: 37662-2401-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 2 NDC: 37662-2401-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/18/2023 3 NDC: 37662-2401-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 4 NDC: 37662-2401-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/18/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2397, 37662-2398, 37662-2399, 37662-2400, 37662-2401, 37662-2402, 37662-2403)
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