Label: RET SMALL INTESTINE 7010- ret small intestine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-7010-1 - 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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INGREDIENTS AND APPEARANCE
RET SMALL INTESTINE 7010
ret small intestine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-7010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (CICHORIUM INTYBUS FLOWER - UNII:HW54500A89) CICHORIUM INTYBUS FLOWER 3 [hp_X] in 29.5 mL CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (CLEMATIS VITALBA FLOWER - UNII:7SCP4N87CI) CLEMATIS VITALBA FLOWER 3 [hp_X] in 29.5 mL ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (ORNITHOGALUM UMBELLATUM FLOWERING TOP - UNII:CZD6M4PY4B) ORNITHOGALUM UMBELLATUM FLOWERING TOP 3 [hp_X] in 29.5 mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X] in 29.5 mL GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 30 [hp_X] in 29.5 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 30 [hp_X] in 29.5 mL LIQUID PETROLEUM (UNII: 6ZAE7X688J) (LIQUID PETROLEUM - UNII:6ZAE7X688J) LIQUID PETROLEUM 30 [hp_X] in 29.5 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_X] in 29.5 mL SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (SCABIES LESION LYSATE (HUMAN) - UNII:5UAU16Z1U4) SCABIES LESION LYSATE (HUMAN) 30 [hp_X] in 29.5 mL PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (PULSATILLA MONTANA WHOLE - UNII:24K790T39B) PULSATILLA MONTANA WHOLE 30 [hp_X] in 29.5 mL DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM 30 [hp_X] in 29.5 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:63083-7010-1 29.5 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(63083-7010)