ARNICA MONTANA- arnica montana tablet

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

Werkstoffen:

ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)

Beschikbaar vanaf:

Schwabe North America

INN (Algemene Internationale Benaming):

ARNICA MONTANA

Samenstelling:

ARNICA MONTANA 6 [hp_X]

Toedieningsweg:

SUBLINGUAL

Prescription-type:

OTC DRUG

therapeutische indicaties:

Temporarily relieves minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion.  For the temporary relief of minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion. 

Autorisatie-status:

unapproved homeopathic

Productkenmerken

ARNICA MONTANA - ARNICA MONTANA TABLET
SCHWABE NORTH AMERICA
_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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ARNICA MONTANA 6X
ACTIVE INGREDIENT
Arnica montana 6X
INACTIVE INGREDIENT
CELLULOSE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
SODIUM CROSCARMELLOSE
DOSAGE & ADMINISTRATION
DOSAGE:
Adults or children over 2 years: Take 3 tablets 4-6 times a day.
Allow to dissolve under tongue.
INDICATIONS
Temporarily relieves minor muscle or joint aches and pain; strains,
sprains, bruises, backache or over-
exertion.
PURPOS E
For the temporary relief of minor muscle or joint aches and pain;
strains, sprains, bruises, backache or
over-exertion.
WARNING
Do not take this product for pain for more than 10 days (adult) or 5
days (children) unless directed by a
doctor.
WHEN USING
When using this product if pain persists or gets worse, if new
symptoms occur, or if redness or
swelling is present, consult a doctor because these could be signs of
a serious condition.
PREGNANCY AND BREAST FEEDING
If pregnant or breast-feeding, ask a health professional before use.
KEEP OUT OF REACH OF CHILDREN.
Keep out of reach of children.
OVERDOS AGE
In case of overdose, seek medical help or contact a Poison Control
Center immediately.
ARNICA MONTANA
arnica montana tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:5349 9 -3533
ROUTE OF ADMINISTRATION
SUBLINGUAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ARNICA MO NTANA (UNII: O8 0 TY20 8 ZW) (ARNICA MONTANA - UNII:O8 0
TY20 8 ZW)
ARNICA MONTANA
6 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
CELLULO SE, MICRO CRYSTALLINE (UNII: OP1R32D6 1U)
LACTO SE MO NO HYDRATE (UNII: EWQ57Q8 I5X)
MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )
CRO SCARMELLO SE SO DIUM (UNII: M28 OL1HH48 )
PRODUCT CHARACTERISTICS
COLOR
white (white tablet)
S CORE
no sco re
S HAP E
ROUND (B&T)
S IZ E
6 mm