KALI MURIATICUM pellet

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)

Available from:

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

USES: Temporary Relief - Occasional Constipation* * Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Condition listed above or as directed by the physician

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                KALI MURIATICUM- KALI MURIATICUM PELLET
RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC
_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._
----------
ACTIVE INGREDIENT
KALI MURIATICUM HPUS 1X and higher
USES
USES: Temporary Relief - Occasional Constipation*
* Claims based on traditional homeopathic practice, not accepted
medical evidence. Not
FDA evaluated.
INDICATIONS
Condition listed above or as directed by the physician
DOSAGE
Adults- Take 4 or 6 Pellets by mouth, three times daily or as
suggested by physician.
Children 2 years and older- take 1/2 the adult dose.
WARNINGS
This product is to be used for self-limiting conditions
If symptoms do not improve in 4 days, or worsen, discontinue use and
seek assistance
of health professional
As with any drug, if you are preganant, or nursing a baby, seek
professional advice
before taking this product
Keep this and all medication out of reach of children
Do not use if capseal is broken or missing.
Close the cap tightly after use.
INACTIVE INGREDIENTS
Sucrose
STORAGE
Store in a cool dark place
QUESTIONS OR COMMENTS
www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com
Rxhomeo, Inc 3200 Commander Dr, Ste 100-W1, Carrollton, TX 75006 USA
KALI MURIATICUM
kali muriaticum pellet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:15631-0251
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION -
UNII:295O53K152)
POTASSIUM CATION
1 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SUCROSE (UNII: C151H8M554)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:15631-
0251-0
100 in 1 PACKAGE; Type 0: Not a Combination
Product
01/01/2018
2
NDC:15631-
0251-1
200 in 1 PACKAGE; Type 0: Not a Combination
Product
01/01/2018
3
NDC:15631-
0251-2
400 in 1 PACKAGE; Type 0: Not a Combinat
                                
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