Label: IMMUNO COMPOUND HOMEOPATHIC TONIC- alfalfa, avena sativa flowering top, oyster shell calcium carbonate, crude, goldenseal, salix nigra bark liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 61750-0022-4, 61750-0022-8 - Packager: HRC Laboratories, Inc.
- 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 March 3, 2018
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- Package Label - 8oz
- Package Lable - 4oz
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INGREDIENTS AND APPEARANCE
IMMUNO COMPOUND HOMEOPATHIC TONIC
alfalfa, avena sativa flowering top, oyster shell calcium carbonate, crude, goldenseal, salix nigra bark liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61750-0022 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD) ALFALFA 1 [hp_X] in 236.6 mL AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP 1 [hp_X] in 236.6 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 1 [hp_X] in 236.6 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 1 [hp_X] in 236.6 mL SALIX NIGRA BARK (UNII: QU52J3A5B3) (SALIX NIGRA BARK - UNII:QU52J3A5B3) SALIX NIGRA BARK 1 [hp_X] in 236.6 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:61750-0022-8 236.6 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/17/2014 2 NDC:61750-0022-4 118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/14/2011 Labeler - HRC Laboratories, Inc. (946106754) Establishment Name Address ID/FEI Business Operations HRC Laboratories, Inc. 946106754 manufacture(61750-0022)