Label: ELAEAGNUS ANGUSTIFLORA pellet
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NDC Code(s):
37662-2910-1,
37662-2910-2,
37662-2910-3,
37662-2911-1, view more37662-2911-2, 37662-2911-3, 37662-2912-1, 37662-2912-2, 37662-2912-3, 37662-2912-4, 37662-2913-1, 37662-2913-2, 37662-2913-3, 37662-2913-4, 37662-2914-1, 37662-2914-2, 37662-2914-3, 37662-2914-4, 37662-2915-1, 37662-2915-2, 37662-2915-3, 37662-2915-4, 37662-2916-1, 37662-2916-2, 37662-2916-3, 37662-2916-4, 37662-2917-1, 37662-2917-2, 37662-2917-3, 37662-2917-4
- 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 March 31, 2023
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
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INGREDIENTS AND APPEARANCE
ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2910 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2910-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2910-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2910-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2912 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2912-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2912-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2912-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2912-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2913 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2913-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2913-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2913-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2913-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2911 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2911-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2911-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2911-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2917 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2917-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2917-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2917-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2917-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2914 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2914-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2914-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2914-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2914-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2915 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2915-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2915-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2915-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2915-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 ELAEAGNUS ANGUSTIFLORA
elaeagnus angustiflora pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2916 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELAEAGNUS ANGUSTIFOLIA WHOLE (UNII: 0RT0F1AT47) (ELAEAGNUS ANGUSTIFOLIA WHOLE - UNII:0RT0F1AT47) ELAEAGNUS ANGUSTIFOLIA 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:37662-2916-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 2 NDC:37662-2916-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/05/2023 3 NDC:37662-2916-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 4 NDC:37662-2916-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/05/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2910, 37662-2911, 37662-2912, 37662-2913, 37662-2914, 37662-2915, 37662-2916, 37662-2917)
