Label: CONSTIPATION RELIEF- alumina, bryonia, graphites, natrum muriaticum, silicea liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-857-01 - Packager: WOONSOCKET PRESCR CTR 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 30, 2014
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active Ingredients Purposes
Alumina 8X .......................................... Hard Stool
Bryonia 8X .......................................... Large Stool
Graphites 8X ......................... Ineffective Discharge
Natrum Muriaticum 8X ......................... Hard Stool
Silicea 8X ...................................... Slow Discharge
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- WARNINGS
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CONSTIPATION RELIEF
alumina, bryonia, graphites, natrum muriaticum, silicea liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-857 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 8 [hp_X] in 30 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 8 [hp_X] in 30 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 8 [hp_X] in 30 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 8 [hp_X] in 30 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 8 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-857-01 30 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/30/2014 Labeler - WOONSOCKET PRESCR CTR INC (062312574) Establishment Name Address ID/FEI Business Operations Apotheca Inc 051457844 manufacture(59779-857)