Label: EUCALYPTUS GLOBULUS pellet
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NDC Code(s):
37662-0681-1,
37662-0681-2,
37662-0681-3,
37662-0682-1, view more37662-0682-2, 37662-0682-3, 37662-0683-1, 37662-0683-2, 37662-0683-3, 37662-0683-4, 37662-0684-1, 37662-0684-2, 37662-0684-3, 37662-0684-4, 37662-0685-1, 37662-0685-2, 37662-0685-3, 37662-0685-4, 37662-0686-1, 37662-0686-2, 37662-0686-3, 37662-0686-4, 37662-0687-1, 37662-0687-2, 37662-0687-3, 37662-0687-4
- 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 June 21, 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
EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0685 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0685-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0685-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0685-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 4 NDC:37662-0685-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0686 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0686-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0686-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0686-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 4 NDC:37662-0686-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0684 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0684-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0684-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0684-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 4 NDC:37662-0684-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0683 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0683-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0683-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0683-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 4 NDC:37662-0683-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0682 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0682-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0682-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0682-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0681 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0681-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0681-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0681-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 EUCALYPTUS GLOBULUS
eucalyptus globulus pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-0687 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 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:37662-0687-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 2 NDC:37662-0687-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/21/2022 3 NDC:37662-0687-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 4 NDC:37662-0687-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0681, 37662-0682, 37662-0683, 37662-0684, 37662-0685, 37662-0686, 37662-0687)
