FERRUM PHOSPHORICUM 6

Main information

  • Trade name:
  • FERRUM PHOSPHORICUM 6- ferrum phosphoricum 6 powder
  • Composition:
  • FERROSOFERRIC PHOSPHATE 6 [hp_X] in 1 g
  • Administration route:
  • ORAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Homeopathic medication

Documents

Localization

  • Available in:
  • FERRUM PHOSPHORICUM 6- ferrum phosphoricum 6 powder
    United States
  • Language:
  • English

Therapeutic information

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

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • unapproved homeopathic
  • Authorization number:
  • 48951-4059-4
  • Last update:
  • 04-06-2019

Summary of Product characteristics: dosage, interactions, side effects

FERRUM PHOSPHORICUM 6- ferrum phosphoricum 6 powder

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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Ferrum phosphoricum 6

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult

a doctor.

Active Ingredient: Ferrum phosphoricum (Nat. ferrous phosphate) 6X

Inactive Ingredient: Lactose

Use: Temporary relief of cough.

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. Contains lactose. 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.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

FERRUM PHOSPHORICUM 6

ferrum phosphoricum 6 powder

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-40 59

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

FERRO SO FERRIC PHO SPHATE (UNII: 9 1GQH8 I5F7) (FERROSOFERRIC PHOSPHATE -

UNII:9 1GQH8 I5F7)

FERROSOFERRIC

PHOSPHATE

6 [hp_X]

in 1 g

Inactive Ingredients

Ingredient Name

Stre ng th

LACTO SE (UNII: J2B2A4N9 8 G)

Uriel Pharmacy Inc.

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:48 9 51-40 59 -

50 g in 1 BOTTLE, GLASS; Type 0 : No t a Co mbinatio n

Pro duc t

0 9 /0 1/20 0 9

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 51-40 59 )

Revised: 4/2018