Label: ILEOCECAL VALVE SUPPORT (iodium, hypophysis suis, thyroidinum, (suis), glandula suprarenalis suis, fel tauri, taraxacum officinale, bryonia (alba), carbo vegetabilis, colocynthis, indolum, lycopodium clavatum, mercurius corrosivus, nux vomica, phosphorus, pulsatilla- vulgaris liquid
- NDC Code(s): 43742-0821-1
- Packager: Deseret Biologicals, 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 September 12, 2022
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ACTIVE INGREDIENTS:
Iodium 6X, Hypophysis Suis 8X, Thyroidinum (Suis) 8X, Glandula Suprarenalis Suis 10X, Fel Tauri 12X, Taraxacum Officinale 12X, Bryonia (Alba) 30C, Carbo Vegetabilis 30C, Colocynthis 30C, Indolum 30C, Lycopodium Clavatum 30C, Mercurius Corrosivus 30C, Nux Vomica 30C, Phosphorus 30C, Pulsatilla (Vulgaris) 30C.
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HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to Ileocecal Valve dysfunction including pelvic pain, fever, headache, bad breath, ringing in the ears, occasional diarrhea, and occasional constipation.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
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HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to Ileocecal Valve dysfunction including pelvic pain, fever, headache, bad breath, ringing in the ears, occasional diarrhea, and occasional constipation.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ILEOCECAL VALVE SUPPORT
iodium, hypophysis suis, thyroidinum, (suis), glandula suprarenalis suis, fel tauri, taraxacum officinale, bryonia (alba), carbo vegetabilis, colocynthis, indolum, lycopodium clavatum, mercurius corrosivus, nux vomica, phosphorus, pulsatilla (vulgaris) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0821 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 6 [hp_X] in 1 mL SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT) SUS SCROFA PITUITARY GLAND 8 [hp_X] in 1 mL SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) SUS SCROFA THYROID 8 [hp_X] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 10 [hp_X] in 1 mL BOS TAURUS BILE (UNII: ET3651ZLOU) (BOS TAURUS BILE - UNII:ET3651ZLOU) BOS TAURUS BILE 12 [hp_X] in 1 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 12 [hp_X] in 1 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 30 [hp_C] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 30 [hp_C] in 1 mL CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 30 [hp_C] in 1 mL INDOLE (UNII: 8724FJW4M5) (INDOLE - UNII:8724FJW4M5) INDOLE 30 [hp_C] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 30 [hp_C] in 1 mL MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 30 [hp_C] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 30 [hp_C] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_C] in 1 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS 30 [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:43742-0821-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/03/2016 08/07/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/03/2016 08/07/2024 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0821) , api manufacture(43742-0821) , label(43742-0821) , pack(43742-0821)