Label: COUGH AND COLD RELIEF- drosera rotundifolia, arsenicum album, ipecacuanha, kali bichromicum, belladonna, pulsatilla, mercurius solubilis liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-2005-4 - 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
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- 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
COUGH AND COLD RELIEF
drosera rotundifolia, arsenicum album, ipecacuanha, kali bichromicum, belladonna, pulsatilla, mercurius solubilis liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-2005 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA 9 [hp_X] in 30 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 9 [hp_X] in 30 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 9 [hp_X] in 30 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 9 [hp_X] in 30 mL ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J) (ATROPA BELLADONNA WHOLE - UNII:DSV74G1P2J) ATROPA BELLADONNA WHOLE 9 [hp_X] in 30 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 9 [hp_X] in 30 mL MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 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:60512-2005-4 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(60512-2005)