Label: COMBINATION REMEDY 6 - UPSET STOMACH- antimonium crudum 6x, antimonium tartaricum 6x, argentum nitricum 6x, china officinalis 3x, kali bichromicum 6x, lycopodium 3x, nux vomica 3x, phosphorus 6x solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 69008-4006-1 - Packager: Warsan Homoeopathic Laboratories
- 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 December 25, 2017
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INGREDIENTS AND APPEARANCE
COMBINATION REMEDY 6 - UPSET STOMACH
antimonium crudum 6x, antimonium tartaricum 6x, argentum nitricum 6x, china officinalis 3x, kali bichromicum 6x, lycopodium 3x, nux vomica 3x, phosphorus 6x solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69008-4006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY TRISULFIDE 6 [hp_X] in 1 mL ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 6 [hp_X] in 1 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 6 [hp_X] in 1 mL CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 3 [hp_X] in 1 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_X] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 3 [hp_X] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 3 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 6 [hp_X] in 1 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:69008-4006-1 20 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 11/16/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/15/2017 Labeler - Warsan Homoeopathic Laboratories (645579772) Registrant - Warsan Homoeopathic Laboratories (645579772) Establishment Name Address ID/FEI Business Operations Warsan Homoeopathic Laboratories 645579772 manufacture(69008-4006) , pack(69008-4006) , label(69008-4006)