Label: THYROPAR (fucus vesiculosus, spongia tosta, glandula suprarenalis suis, hypophysis suis, thyroidinum (suis), bromium, calcarea carbonica, graphites, iodium, lachesis mutus, levothyroxinum, pulsatilla- pratensis, selenium metallicum liquid
- NDC Code(s): 44911-0683-1
- Packager: Energique, 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 October 26, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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ACTIVE INGREDIENTS:
(in each drop) Bromium 12X 9.07%, Calcarea Carbonica 12X 9.07%, Glandula Suprarenalis Suis 6X 9.07%, Graphites 12X 9.07%, Hypophysis Suis 6X 9.07%, Iodium 12X 9.07%, Lachesis Mutus 12X 9.07%, Levothyroxinum 12X 9.07%, Pulsatilla 12X 9.07%, Selenium Metallicum 12X 9.07%, Thyroidinum 6X 9.07%, Fucus Vesiculosus 3X 0.10%, Spongia Tosta 3X 0.10%.
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PURPOSE:
Bromium – neck swelling,** Calcarea Carbonica 12X - constipation,** Glandula Suprarenalis Suis - fatigue,** Graphites – dry skin,** Hypophysis Suis – heavy menses,** Iodium - forgetfulness,** Lachesis Mutus - insomnia,** Levothyroxinum - chilliness,** Pulsatilla - sadness,** Selenium Metallicum – hair loss,** Thyroidinum - edema,** Fucus Vesiculosus – weight gain,** Spongia Tosta - soreness.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
- USES:
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WARNINGS:
Stop use and ask a doctor if symptoms persist for more than 7 days.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING
Store in a cool, dry place.
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
THYROPAR
fucus vesiculosus, spongia tosta, glandula suprarenalis suis, hypophysis suis, thyroidinum (suis), bromium, calcarea carbonica, graphites, iodium, lachesis mutus, levothyroxinum, pulsatilla (pratensis), selenium metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0683 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X] in 1 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 6 [hp_X] in 1 mL SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT) SUS SCROFA PITUITARY GLAND 6 [hp_X] in 1 mL THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) THYROID 6 [hp_X] in 1 mL BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G) BROMINE 12 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 1 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 12 [hp_X] in 1 mL IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 12 [hp_X] in 1 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 12 [hp_X] in 1 mL LEVOTHYROXINE (UNII: Q51BO43MG4) (LEVOTHYROXINE - UNII:Q51BO43MG4) LEVOTHYROXINE 12 [hp_X] in 1 mL PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 12 [hp_X] in 1 mL SELENIUM (UNII: H6241UJ22B) (SELENIUM - UNII:H6241UJ22B) SELENIUM 12 [hp_X] 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:44911-0683-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 10/26/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/26/2023 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0683) , api manufacture(44911-0683) , label(44911-0683) , pack(44911-0683)
