QUARTZ 8 liquid

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Principio attivo:

SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)

Commercializzato da:

Uriel Pharmacy Inc.

INN (Nome Internazionale):

SILICON DIOXIDE

Composizione:

SILICON DIOXIDE 8 [hp_X] in 1 mL

Via di somministrazione:

ORAL

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

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

Stato dell'autorizzazione:

unapproved homeopathic

Scheda tecnica

QUARTZ 8- QUARTZ 8 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._
----------
QUARTZ 8
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredient: Quartz (Rock crystal) 8X
Inactive Ingredients: Water, Salt, Lactose
"prepared using rhythmical processes"
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. Contains traces of lactose. 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 shopuriel.com
Lot:
QUARTZ 8
quartz 8 liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-8109
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
SILICON DIOXIDE
8 [hp_X] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:48951-
8109-1
10 in 1 BOX
09/01/2009
1
1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-
Package
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved
homeopathic
09/01/2009
LABELER -
Uriel Pharmacy Inc. (043471163)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Uriel Pharmacy Inc.
043471163
manufacture(48951-8109)
Revised: 4/2024