Label: COMBINATION REMEDY 9 - INDIGESTION- antimonium crudum, arsenicum album, carbo vegetabilis , china officinalis, gentiana lutea, hydrastis canadensis, nux vomica solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 69008-4009-1 - 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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- ACTIVE INGREDIENT
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
COMBINATION REMEDY 9 - INDIGESTION
antimonium crudum, arsenicum album, carbo vegetabilis , china officinalis, gentiana lutea, hydrastis canadensis, nux vomica solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69008-4009 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 ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 3 [hp_X] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 8 [hp_X] in 1 mL GENTIANA LUTEA ROOT (UNII: S72O3284MS) (GENTIANA LUTEA ROOT - UNII:S72O3284MS) GENTIANA LUTEA ROOT 3 [hp_X] in 1 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 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 CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 3 [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:69008-4009-1 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(69008-4009) , pack(69008-4009) , label(69008-4009)