NATRUM PHOSPHORICUM pellet

Nchi: Marekani

Lugha: Kiingereza

Chanzo: NLM (National Library of Medicine)

Nunua Sasa

Tabia za bidhaa Tabia za bidhaa (SPC)
24-10-2013

Viambatanisho vya kazi:

SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) (PHOSPHATE ION - UNII:NK08V8K8HR)

Inapatikana kutoka:

HOMEOLAB USA INC.

Njia ya uendeshaji:

ORAL

Dawa ya aina:

OTC DRUG

Matibabu dalili:

HYPERACIDITY, MOUTH ULCERS For self-limiting condition listed above or as directed by a health professional.

Idhini hali ya:

unapproved homeopathic

Tabia za bidhaa

                                NATRUM PHOSPHORICUM- NATRUM PHOSPHORICUM PELLET
HOMEOLAB USA 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._
----------
HOMEOPATHIC MEDICINE NDC 60512-6346-1
ACTIVE INGREDIENT HPUS
NATRUM PHOSPHORICUM 1X
(Sodium Phosphate, dibasic)
HYPERACIDITY, MOUTH ULCERS
USE
For self-limiting condition listed above or as directed by a health
professional.
WARNINGS
DO NOT USE if pellet-dispenser seal is broken.
STOP USE AND ASK A DOCTOR IF symptoms persist more than 3 days or
worsen.
IF PREGNANT OR BREAST-FEEDING, ask a health professional before use.
KEEP OUT OF REACH OF CHILDREN.
DIRECTIONS
ADULTS: Allow 3 or 4 pellets to dissolve in the mouth 3 times a day
until symptoms are relieved or as
directed by a health professional.
OTHER INFORMATION
Store at room temperature.
INACTIVE INGREDIENTS
Lactose, sucrose.
QUESTIONS?
1-800-404-4666
_The letters 'HPUS' indicate that the component in this product is
officially monographed in the Homeopathic_
_Pharmacopoeia of the United States._
_These claims have not been reviewed by the Food and Drug
Administration. They are based on traditional_
_homeopathic practice._
80 Pellets
Pellet dispenser
Mfd for: HOMEOLAB USA INC., 3025 De L`Assomption, Montreal, QC, H1N
2H2, CANADA
Product of Canada
LABEL
NATRUM PHOSPHORICUM
natrum phosphoricum pellet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 0 512-6 346
ROUTE OF ADMINISTRATION
ORAL
HOMEOLAB USA INC.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SO DIUM PHO SPHATE, DIBASIC (UNII: GR6 8 6 LBA74) (PHOSPHATE ION -
UNII:NK0 8 V8 K8 HR)
SODIUM PHOSPHATE,
DIBASIC
1 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
LACTO SE (UNII: J2B2A4N9 8 G)
SUCRO SE (UNII: C151H8 M554)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:6 0 512-6 346 -1
8 0 in 1 TUBE
MARKETING INFORMATION
MARKE TING CATE GO
                                
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