Label: RET HEART 7009- ret heart liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-7009-1 - 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 HEART 7009
ret heart liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-7009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (FAGUS SYLVATICA FLOWERING TOP - UNII:21AF0IHY5U) FAGUS SYLVATICA FLOWERING TOP 3 [hp_X] in 29.5 mL IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (IMPATIENS GLANDULIFERA FLOWER - UNII:AJU5O1A5ZV) IMPATIENS GLANDULIFERA FLOWER 3 [hp_X] in 29.5 mL VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ) (VERBENA OFFICINALIS FLOWERING TOP - UNII:311PNK9CDZ) VERBENA OFFICINALIS FLOWERING TOP 3 [hp_X] in 29.5 mL POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (POTASSIUM PHOSPHATE, UNSPECIFIED FORM - UNII:B7862WZ632) POTASSIUM PHOSPHATE, UNSPECIFIED FORM 3 [hp_X] in 29.5 mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 3 [hp_X] in 29.5 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 3 [hp_X] in 29.5 mL ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS WHOLE - UNII:U0NQ8555JD) ACONITUM NAPELLUS WHOLE 30 [hp_X] in 29.5 mL GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 30 [hp_X] in 29.5 mL CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 30 [hp_X] in 29.5 mL COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (COFFEA ARABICA SEED, ROASTED - UNII:9H58JRT35E) COFFEA ARABICA SEED, ROASTED 30 [hp_X] in 29.5 mL SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ) SAFFRON 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 Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-7009-1 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(63083-7009)