Label: ENDOPURE ESTRO (estradiol, estriol, folliculinum, belladonna, chelidonium majus, glandula suprarenalis suis, hydrocortisone (cortisol), hypothalamus suis, oophorinum (suis), pineal (suis), hypophysis (suis), sanguinaria canadensis, lilium tigrinum, pulsatilla- vulgaris, sepia, sulphur liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 50181-0067-1 - Packager: The Wellness Center for Research and Education
- 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 April 11, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENTS:
Estradiol 6X, Estriol 6X, Folliculinum 6X, Belladonna 6C, Chelidonium Majus 6C, Glandula Suprarenalis Suis 6C, Hydrocortisone (Cortisol) 6C, Hypothalamus Suis 6C, Oophorinum (Suis) 6C, Pineal (Suis) 6C, Hypophysis (Suis) 6C, Sanguinaria Canadensis 6C, Lilium Tigrinum 12C, Pulsatilla (Vulgaris) 12C, Sepia 12C, Sulphur 12C.
- HOMEOPATHIC INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
-
DIRECTIONS:
5 drops orally 2 to 3 times daily between meals. Administer orally, day 1 through 24 of the monthly menstrual cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first of the calendar month. Use between 7:30 and 8:30 pm and upon waking. Consult a physician for use in children under 12 years of age.
- HOMEOPATHIC INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
-
INGREDIENTS AND APPEARANCE
ENDOPURE ESTRO
estradiol, estriol, folliculinum, belladonna, chelidonium majus, glandula suprarenalis suis, hydrocortisone (cortisol), hypothalamus suis, oophorinum (suis), pineal (suis), hypophysis (suis), sanguinaria canadensis, lilium tigrinum, pulsatilla (vulgaris), sepia, sulphur liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50181-0067 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ESTRADIOL (UNII: 4TI98Z838E) (ESTRADIOL - UNII:4TI98Z838E) ESTRADIOL 6 [hp_X] in 1 mL ESTRIOL (UNII: FB33469R8E) (ESTRIOL - UNII:FB33469R8E) ESTRIOL 6 [hp_X] in 1 mL ESTRONE (UNII: 2DI9HA706A) (ESTRONE - UNII:2DI9HA706A) ESTRONE 6 [hp_X] in 1 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 6 [hp_C] in 1 mL CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS 6 [hp_C] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 6 [hp_C] in 1 mL HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 6 [hp_C] in 1 mL SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (SUS SCROFA HYPOTHALAMUS - UNII:N6R0856Z79) SUS SCROFA HYPOTHALAMUS 6 [hp_C] in 1 mL SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O) SUS SCROFA OVARY 6 [hp_C] in 1 mL SUS SCROFA PINEAL GLAND (UNII: 050QZ2EDK7) (SUS SCROFA PINEAL GLAND - UNII:050QZ2EDK7) SUS SCROFA PINEAL GLAND 6 [hp_C] in 1 mL SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT) SUS SCROFA PITUITARY GLAND 6 [hp_C] in 1 mL SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT 6 [hp_C] in 1 mL LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (LILIUM LANCIFOLIUM WHOLE FLOWERING - UNII:X67Z2963PI) LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_C] in 1 mL ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA 12 [hp_C] in 1 mL SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 12 [hp_C] in 1 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_C] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50181-0067-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 04/11/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/11/2019 Labeler - The Wellness Center for Research and Education (832363993) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(50181-0067) , api manufacture(50181-0067) , label(50181-0067) , pack(50181-0067)