Label: AM-3- cinchona officinalis bark, potassium chlorate, and lachesis muta whole solution
- NDC Code(s): 58264-0342-1
- Packager: DNA Labs, 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 June 1, 2022
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INGREDIENTS AND APPEARANCE
AM-3
cinchona officinalis bark, potassium chlorate, and lachesis muta whole solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0342 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 10 [hp_X] in 1 mL POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORATE ION - UNII:08Z8093742) POTASSIUM CHLORATE 8 [hp_X] in 1 mL LACHESIS MUTA WHOLE (UNII: 6Y582I290C) (LACHESIS MUTA WHOLE - UNII:6Y582I290C) LACHESIS MUTA WHOLE 12 [hp_X] in 1 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:58264-0342-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/1990 Labeler - DNA Labs, Inc. (031784339)