ECHINACEA ARGENTUM liquid

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

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Active ingredient:
ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX), ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4), SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)
Available from:
Uriel Pharmacy Inc.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Directions: FOR ORAL USE. Use: Temporary relief of headache.
Authorization status:
unapproved homeopathic
Authorization number:
48951-4155-1

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, Boric acid, 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

ECHINACEA ARGENTUM

echinacea argentum liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-4155

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ECHINACEA, UNSPECIFIED (UNII: 4N9 P6 CC1DX) (ECHINACEA, UNSPECIFIED -

UNII:4N9 P6 CC1DX)

ECHINACEA,

UNSPECIFIED

3 [hp_X]

in 1 mL

ATRO PA BELLADO NNA (UNII: WQZ3G9 PF0 H) (ATROPA BELLADONNA -

UNII:WQZ3G9 PF0 H)

ATROPA

BELLADONNA

20 [hp_X]

in 1 mL

20 [hp_X]

Uriel Pharmacy Inc.

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6 XBU4)

SILICON DIOXIDE

20 [hp_X]

in 1 mL

SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)

SILVER

30 [hp_X]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

SO DIUM BICARBO NATE (UNII: 8 MDF5V39 QO)

WATER (UNII: 0 59 QF0 KO0 R)

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)

BO RIC ACID (UNII: R57ZHV8 5D4)

RO SE O IL (UNII: WUB6 8 Y35M7)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:48 9 51-

4155-1

1 in 1 BAG

0 9 /0 1/20 0 9

1

10 mL in 1 BOTTLE, DROPPER; Type 0 : No t a Co mbinatio n

Pro duc t

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 /0 1/20 0 9

Labeler -

Uriel Pharmacy Inc. (043471163)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Uriel Pharmacy Inc.

0 4347116 3

ma nufa c ture (48 9 51-4155)

Revised: 9/2019

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