Label: ULCER DROPS 2094- ulcer drops liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-2094-2 - Packager: Professional Complementary Health Formulas
- 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 August 15, 2019
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WARNINGS
Severe or persistent symptoms may be a sign of a serious condition. Consult a doctor promptly if symptoms persist or are accompanied by a fever, vomiting, diarrhea, or loss of appetite. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.
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INGREDIENTS AND APPEARANCE
ULCER DROPS 2094
ulcer drops liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-2094 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H) GLYCYRRHIZA GLABRA 2 [hp_X] in 59 mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 2 [hp_X] in 59 mL STARCH, RICE (UNII: 4DGK8B7I3S) (STARCH, RICE - UNII:4DGK8B7I3S) STARCH, RICE 2 [hp_X] in 59 mL PANICUM MILIACEUM WHOLE (UNII: 072D7X60WS) (PANICUM MILIACEUM WHOLE - UNII:072D7X60WS) PANICUM MILIACEUM WHOLE 2 [hp_X] in 59 mL PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8) (PLANTAGO LANCEOLATA LEAF - UNII:2YWL9J7EE8) PLANTAGO LANCEOLATA LEAF 2 [hp_X] in 59 mL FU LING (UNII: XH37TWY5O4) (FU LING - UNII:XH37TWY5O4) FU LING 2 [hp_X] in 59 mL DAIKON (UNII: 86R5J6D01D) (DAIKON - UNII:86R5J6D01D) DAIKON 2 [hp_X] in 59 mL BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (BLACK MUSTARD SEED - UNII:8LTY55LQ8D) BLACK MUSTARD SEED 2 [hp_X] in 59 mL ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (ELYMUS REPENS ROOT - UNII:3IXW0F6P8W) ELYMUS REPENS ROOT 2 [hp_X] in 59 mL GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 2 [hp_X] in 59 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 5 [hp_X] in 59 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 6 [hp_X] in 59 mL COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 6 [hp_X] in 59 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 12 [hp_X] in 59 mL HELICOBACTER PYLORI (UNII: U09W5JOL3Z) (HELICOBACTER PYLORI - UNII:U09W5JOL3Z) HELICOBACTER PYLORI 30 [hp_X] in 59 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:63083-2094-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-2094)
