ECHINACEA ARGENTUM liquid

Country: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
06-05-2021

Virkt innihaldsefni:

ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX), SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G), ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)

Fáanlegur frá:

Uriel Pharmacy Inc.

Stjórnsýsluleið:

ORAL

Gerð lyfseðils:

OTC DRUG

Ábendingar:

Directions: FOR ORAL USE. Use: Temporary relief of headache.

Leyfisstaða:

unapproved homeopathic

Vara einkenni

                                ECHINACEA ARGENTUM- ECHINACEA ARGENTUM LIQUID
URIEL PHARMACY 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.
----------
ECHINACEA ARGENTUM
Directions: FOR ORAL USE.
Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops.
Under age 2:
Consult a doctor.
Active Ingredients: Echinacea e pl. tota (Purple coneflower) 3X,
Atropa belladonna ex
herba (Nightshade) 20X, Quartz (Rock crystal) 20X, Argentum met.
(Silver) 30X
Inactive Ingredients: Water, Salt, Sodium bicarbonate, Rose oil
Use: Temporary relief of headache.
KEEP OUT OF REACH OF CHILDREN.
Warnings: Claims based on traditional homeopathic practice, not
accepted medical
evidence. Not FDA evaluated. Do not use if allergic to any ingredient.
Consult a doctor
before use for serious conditions or if conditions worsen or persist.
If pregnant or
nursing, consult a doctor before use. Do not use if safety seal is
broken or missing.
REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
Opened on:_________________
Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot#
ECHINACEA ARGENTUM
echinacea argentum liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-4166
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
Uriel Pharmacy Inc.
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED -
UNII:4N9P6CC1DX)
ECHINACEA,
UNSPECIFIED
3 [hp_X]
in 1 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)
SILVER
30 [hp_X]
in 1 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA -
UNII:WQZ 3G9PF0H)
ATROPA
BELLADONNA
20 [hp_X]
in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
SILICON DIOXIDE
20 [hp_X]
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ROSE OIL (UNII: WUB68Y35M7)
SODIUM BICAR
                                
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