CARPELLUM MALI COMP.

Main information

  • Trade name:
  • CARPELLUM MALI COMP.- carpellum mali comp. liquid
  • Composition:
  • ENGLISH WALNUT 4 [hp_X] in 1 mL
  • Administration route:
  • ORAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Homeopathic medication

Documents

Localization

  • Available in:
  • CARPELLUM MALI COMP.- carpellum mali comp. liquid
    United States
  • Language:
  • English

Therapeutic information

  • Therapeutic indications:
  • Use: Temporary relief of headache.

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • unapproved homeopathic
  • Authorization number:
  • 48951-3034-3
  • Last update:
  • 04-06-2019

Summary of Product characteristics: dosage, interactions, side effects

CARPELLUM MALI COMP.- carpellum mali comp. 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.

----------

Carpellum Mali Comp.

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

Active Ingredients: Juglans regia (Walnut) 4X, Pyrus malus (Lining of apple seed chamber) 4X

Inactive Ingredients: Distilled water, Organic cane alcohol

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. 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.

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

CARPELLUM MALI COMP.

carpellum mali comp. liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-30 34

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7)

ENGLISH WALNUT

4 [hp_X]

in 1 mL

MALUS DO MESTICA WHO LE (UNII: 0 4W6 36 S1V3) (MALUS DOMESTICA WHOLE -

UNII:0 4W6 36 S1V3)

MALUS DOMESTICA

WHOLE

4 [hp_X]

in 1 mL

Uriel Pharmacy Inc.

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

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

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:48 9 51-30 34-

6 0 mL in 1 BOTTLE, DROPPER; 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 51-30 34)

Revised: 4/2018