ARGENTUM QUARTZ liquid

Pays: États-Unis

Langue: anglais

Source: NLM (National Library of Medicine)

Ingrédients actifs:

SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)

Disponible depuis:

Uriel Pharmacy Inc.

DCI (Dénomination commune internationale):

SILVER

Composition:

SILVER 20 [hp_X] in 1 mL

Mode d'administration:

ORAL

Type d'ordonnance:

OTC DRUG

indications thérapeutiques:

Directions: FOR ORAL USE. Use: Temporary relief of ear irritation.

Statut de autorisation:

unapproved homeopathic

Résumé des caractéristiques du produit

ARGENTUM QUARTZ- ARGENTUM QUARTZ 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._
----------
ARGENTUM QUARTZ
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then swallow.
Active Ingredients: Argentum met. (Silver) 20X, Quartz (Rock crystal)
30X
Inactive Ingredients: Water, Salt
Use: Temporary relief of ear irritation.
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.
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
ARGENTUM QUARTZ
argentum quartz liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:48 9 51-10 9 8
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)
SILVER
20 [hp_X] in 1 mL
SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6
XBU4)
SILICON DIOXIDE
30 [hp_X] in 1 mL
Uriel Pharmacy Inc.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:48 9 51-10 9 8 -1
10 in 1 BOX
0 9 /0 1/20 0 9
1
1 mL in 1 AMPULE; 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 /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 51-10 9 8 )
Revised: 4/