CHRYSOLITH 6

Main information

  • Trade name:
  • CHRYSOLITH 6- chrysolith 6 liquid
  • Composition:
  • COLLOIDAL SILICON DIOXIDE 6 [hp_X] in 1 mL
  • Administration route:
  • ORAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Homeopathic medication

Documents

Localization

  • Available in:
  • CHRYSOLITH 6- chrysolith 6 liquid
    United States
  • Language:
  • English

Therapeutic information

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

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • unapproved homeopathic
  • Authorization number:
  • 48951-3085-1
  • Last update:
  • 04-06-2019

Summary of Product characteristics: dosage, interactions, side effects

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.

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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 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 s s

ID/FEI

Busine ss Ope rations

Uriel Pharmacy Inc.

0 4347116 3

ma nufa c ture (48 9 51-30 8 5)

Revised: 4/2018