Label: LARGE INTESTINE FORMULA 2103- large intestine formula liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-2103-2 - 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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INGREDIENTS AND APPEARANCE
LARGE INTESTINE FORMULA 2103
large intestine formula liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-2103 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SCLEROMITRION DIFFUSUM WHOLE (UNII: 291PPU5K9I) (SCLEROMITRION DIFFUSUM WHOLE - UNII:291PPU5K9I) SCLEROMITRION DIFFUSUM WHOLE 1 [hp_X] in 59 mL FERROSOFERRIC OXIDE (UNII: XM0M87F357) (FERROSOFERRIC OXIDE - UNII:XM0M87F357) FERROSOFERRIC OXIDE 1 [hp_X] in 59 mL SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X) (SANGUISORBA OFFICINALIS ROOT - UNII:4NYV2HT01X) SANGUISORBA OFFICINALIS ROOT 1 [hp_X] in 59 mL MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) (MAGNOLIA OFFICINALIS BARK - UNII:5M609NV974) MAGNOLIA OFFICINALIS BARK 1 [hp_X] in 59 mL STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E) (STYPHNOLOBIUM JAPONICUM FLOWER - UNII:644C3CSB6E) STYPHNOLOBIUM JAPONICUM FLOWER 1 [hp_X] in 59 mL SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (SCUTELLARIA BAICALENSIS ROOT - UNII:7J95K7ID2S) SCUTELLARIA BAICALENSIS ROOT 1 [hp_X] in 59 mL LONICERA HYPOGLAUCA FLOWER (UNII: 3ADI26ATFY) (LONICERA HYPOGLAUCA FLOWER - UNII:3ADI26ATFY) LONICERA HYPOGLAUCA FLOWER 1 [hp_X] in 59 mL TARAXACUM SINICUM WHOLE (UNII: 11982A05XX) (TARAXACUM SINICUM WHOLE - UNII:11982A05XX) TARAXACUM SINICUM WHOLE 1 [hp_X] in 59 mL ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (ANGELICA GIGAS ROOT - UNII:32766B2FHX) ANGELICA GIGAS ROOT 3 [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:63083-2103-2 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(63083-2103)