Label: CONSTIPATION RELIEF- croton tiglium, alumina, argentum nitricum, podophyllum peltatum, magnesia carbonica liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-2004-4 - Packager: HOMEOLAB USA 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 November 11, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Homeopathic Liquid Attenuations ACTIVE INGREDIENTS HPUS
- REFERENCES
- PURPOSE
- USES
- WARNINGS
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- CARTON
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INGREDIENTS AND APPEARANCE
CONSTIPATION RELIEF
croton tiglium, alumina, argentum nitricum, podophyllum peltatum, magnesia carbonica liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-2004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (CROTON TIGLIUM SEED - UNII:0HK2GZK66E) CROTON TIGLIUM SEED 9 [hp_X] in 30 mL ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 9 [hp_X] in 30 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 9 [hp_X] in 30 mL PODOPHYLLUM PELTATUM ROOT (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM PELTATUM ROOT 9 [hp_X] in 30 mL MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CARBONATE HYDROXIDE 9 [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:60512-2004-4 30 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/11/2013 Labeler - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-2004)