NATRUM MURIATICUM- natrum muriaticum pellet

United States - English - NLM (National Library of Medicine)

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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:
Dry Mucous Membranes Condition listed above or as directed by the physician
Authorization status:
unapproved homeopathic
Authorization number:
15631-0309-0, 15631-0309-1, 15631-0309-2, 15631-0309-3, 15631-0309-4, 15631-0309-5

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.

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ACTIVE INGREDIENT

NATRUM MURIATICUM HPUS 1X and higher

USES

Dry Mucous Membranes

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 9415 Burnet Road, Suite 312, Austin, TX 78758

NATRUM MURIATICUM

natrum muriaticum pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:156 31-0 30 9

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X) (CHLORIDE ION - UNII:Q32ZN48 6 9 8 )

SODIUM CHLORIDE

1 [hp_X]

Inactive Ingredients

Ingredient Name

Stre ng th

SUCRO SE (UNII: C151H8 M554)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:156 31-0 30 9 -0

10 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

2

NDC:156 31-0 30 9 -1

20 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

3

NDC:156 31-0 30 9 -2

40 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

4

NDC:156 31-0 30 9 -3

750 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

5

NDC:156 31-0 30 9 -4

250 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

6

NDC:156 31-0 30 9 -5

1250 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

0 9 /10 /20 15

Labeler -

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994)

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

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Rxho meo , Inc

8 325349 8 1

who lesale drug distributo r(156 31-0 30 9 )

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Rxho meo Private Limited d.b.a. Rxho meo , Inc

6 50 8 339 9 4

manufacture(156 31-0 30 9 ) , label(156 31-0 30 9 )

Revised: 11/2015

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