CHRYSOLITH 6- chrysolith 6 liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

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

Available from:

Uriel Pharmacy Inc.

INN (International Name):

COLLOIDAL SILICON DIOXIDE

Composition:

COLLOIDAL SILICON DIOXIDE 6 [hp_X] in 1 mL

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE. Use: Temporary relief of light sensitivity.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                CHRYSOLITH 6- CHRYSOLITH 6 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._
----------
CHRYSOLITH 6
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 Ingredient: Chrysolith 6X
Inactive Ingredients: Water, Salt, Sodium bicarbonate, Rose oil
Use: Temporary relief of light sensitivity.
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.
Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com
CHRYSOLITH 6
chrysolith 6 liquid
PRODUCT INFORMATION
Uriel Pharmacy Inc.
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:48 9 51-30 8 5
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6
XBU4)
SILICON DIOXIDE
6 [hp_X] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
SO DIUM BICARBO NATE (UNII: 8 MDF5V39 QO)
RO SE O IL (UNII: WUB6 8 Y35M7)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:48 9 51-30 8 5-
1
1 in 1 BAG
0 9 /0 1/20 0 9
1
7 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 
                                
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