NATRUM MURIATICUM pellet

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Buy It Now

Active ingredient:

SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)

Available from:

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

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

USES: Temporary Relief - Headache* * 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

                                NATRUM MURIATICUM- NATRUM 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
NATRUM MURIATICUM HPUS 1X and higher
USES
USES: Temporary Relief - Headache*
* 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
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
NATRUM MURIATICUM
natrum muriaticum pellet
PRODUCT INFORMATION
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:15631-0309
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH STRENGTH
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)
SODIUM CHLORIDE
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-
0309-0
100 in 1 PACKAGE; Type 0: Not a Combination
Product
01/01/2018
2
NDC:15631-
0309-1
200 in 1 PACKAGE; Type 0: Not a Combination
Product
01/01/2018
3
NDC:15631-
0309-2
400 in 1 PACKAGE; Type 0: Not a Combination
Product
01/01/2018
4
NDC:15631-
0309-3
750
                                
                                Read the complete document
                                
                            

Search alerts related to this product