LITHIUM- lithium bromatum liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

Lithium Bromatum 3xHPUS, The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates., For the temporary relief of symptoms due to depression, anxiety, and vertigo., Keep out of reach of children., Adults: Take 20 drops on the toungue or in water two to three times daily. Children receive 1/2 of the adult amount., If pregnant or breast-feeding, consult a health professional before use., (Read Suggested Use Section), Ethyl alcohol

Available from:

Marco Pharma International LLC.

Administration route:

ORAL

Prescription type:

OTC DRUG

Authorization status:

unapproved homeopathic

Summary of Product characteristics

LITHIUM- LITHIUM BROMATUM LIQUID
MARCO PHARMA INTERNATIONAL LLC.
_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 FACTS
ACTIVE INGREDIENTS
Lithium Bromatum 3xHPUS
The letters HPUS indicates that the components in this product are
officially
monographed in the Homeopathic Pharmacopoeia of United Sates.
PURPOSE
For the temporary relief of symptoms due to depression, anxiety, and
vertigo.
Keep out of reach of children.
DOSAGE
Adults: Take 20 drops on the toungue or in water two to three times
daily. Children
receive 1/2 of the adult amount.
WARNINGS
IF PREGNANT OR BREAST-FEEDING, CONSULT a health professional before
use.
(Read Suggested Use Section)
INACTIVE INGREDIENTS
Ethyl alcohol (18% by vol.) and water.
LITHIUM
lithium bromatum liquid
PRODUCT 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
Marco Pharma International LLC.
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)
Revised: 12/2021