ARGENTUM 6

Main information

  • Trade name:
  • ARGENTUM 6- argentum 6 liquid
  • Composition:
  • SILVER 6 [hp_X] in 1 mL
  • Administration route:
  • ORAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Homeopathic medication

Documents

Localization

  • Available in:
  • ARGENTUM 6- argentum 6 liquid
    United States
  • Language:
  • English

Therapeutic information

  • Therapeutic indications:
  • Directions: FOR ORAL USE ONLY. Use: Temporary relief of headache.

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • unapproved homeopathic
  • Authorization number:
  • 48951-1085-3
  • Last update:
  • 03-06-2019

Summary of Product characteristics: dosage, interactions, side effects

ARGENTUM 6- argentum 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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Argentum 6

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Active Ingredient: Argentum metallicum 6X

Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions

or if conditions worsen or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor

before use. Do not use if safety seal is broken or missing.

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

ARGENTUM 6

argentum 6 liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-10 8 5

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

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

SILVER

6 [hp_X] in 1 mL

Inactive Ingredients

Uriel Pharmacy Inc.

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

ALCO HO L (UNII: 3K9 9 58 V9 0 M)

LACTO SE (UNII: J2B2A4N9 8 G)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:48 9 51-10 8 5-3

6 0 mL in 1 BOTTLE, DROPPER

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 8 5)

Revised: 8/2014