Label: LITHIUM- lithium bromatum liquid
- NDC Code(s): 60986-1019-3, 60986-1019-4
- Packager: Marco Pharma International LLC.
- 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 December 3, 2024
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INGREDIENTS AND APPEARANCE
LITHIUM
lithium bromatum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60986-1019 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHIUM BROMIDE (UNII: 864G646I84) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM BROMIDE 3 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60986-1019-3 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2018 2 NDC:60986-1019-4 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/01/1992 Labeler - Marco Pharma International LLC. (161994277) Registrant - Marco Pharma International LLC. (161994277) Establishment Name Address ID/FEI Business Operations Nestmann Pharma GmbH 323426262 manufacture(60986-1019)