Melilotus Officinalis: Homeopathic Product Information

MELILOTUS OFFICINALIS- melilotus officinalis top pellet
Hahnemann Laboratories, INC.

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.

Melilotus Officinalis 6C 5g
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Melilotus Officinalis 6C 30g
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Melilotus Officinalis 6C 100g
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Melilotus Officinalis 12C 5g
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Melilotus Officinalis 12C 30g
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Melilotus Officinalis 12C 100g
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Melilotus Officinalis 30C 1g
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Melilotus Officinalis 30C 5g
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Melilotus Officinalis 30C 30g
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Melilotus Officinalis 30C 100g
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Melilotus Officinalis 100C 1g
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Melilotus Officinalis 100C 5g
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Melilotus Officinalis 100C 30g
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Melilotus Officinalis 100C 100g
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Melilotus Officinalis 200C 1g
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Melilotus Officinalis 200C 5g
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Melilotus Officinalis 200C 30g
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Melilotus Officinalis 200C 100g
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Melilotus Officinalis 500C 1g
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Melilotus Officinalis 500C 5g
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Melilotus Officinalis 500C 30g
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Melilotus Officinalis 500C 100g
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Melilotus Officinalis 1M 1g
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Melilotus Officinalis 1M 5g
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Melilotus Officinalis 1M 30g
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Melilotus Officinalis 1M 100g
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Melilotus Officinalis LM1 30g
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MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1142
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 100 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 2mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1142-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1142-2 500 PELLET in 1 VIAL, GLASS None
3 NDC:37662-1142-3 3000 PELLET in 1 BOTTLE, GLASS None
4 NDC:37662-1142-4 10000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1139
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 6 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 3mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1139-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1139-2 1200 PELLET in 1 BOTTLE, GLASS None
3 NDC:37662-1139-3 4000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1141
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 30 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 3mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1141-1 80 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1141-2 200 PELLET in 1 VIAL, GLASS None
3 NDC:37662-1141-3 1200 PELLET in 1 BOTTLE, GLASS None
4 NDC:37662-1141-4 4000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1140
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 12 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 3mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1140-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1140-2 1200 PELLET in 1 BOTTLE, GLASS None
3 NDC:37662-1140-3 4000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1143
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 200 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 2mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1143-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1143-2 500 PELLET in 1 VIAL, GLASS None
3 NDC:37662-1143-3 3000 PELLET in 1 BOTTLE, GLASS None
4 NDC:37662-1143-4 10000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1144
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 500 [hp_C]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 2mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1144-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1144-2 500 PELLET in 1 VIAL, GLASS None
3 NDC:37662-1144-3 3000 PELLET in 1 BOTTLE, GLASS None
4 NDC:37662-1144-4 10000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1145
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 1 [hp_M]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 2mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1145-1 200 PELLET in 1 VIAL, GLASS None
2 NDC:37662-1145-2 500 PELLET in 1 VIAL, GLASS None
3 NDC:37662-1145-3 3000 PELLET in 1 BOTTLE, GLASS None
4 NDC:37662-1145-4 10000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
MELILOTUS OFFICINALIS
melilotus officinalis pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1146
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELILOTUS OFFICINALIS TOP (MELILOTUS OFFICINALIS TOP) MELILOTUS OFFICINALIS TOP 1 [hp_Q]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 1mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37662-1146-1 10000 PELLET in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/01/2022
Labeler — Hahnemann Laboratories, INC. (147098081)
Establishment
Name Address ID/FEI Operations
Hahnemann Laboratories, INC. 147098081 manufacture (37662-1139), manufacture (37662-1140), manufacture (37662-1141), manufacture (37662-1142), manufacture (37662-1143), manufacture (37662-1144), manufacture (37662-1145), manufacture (37662-1146)

Revised: 08/2022 Hahnemann Laboratories, INC.

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