HEMORRHOIDS PROCTALGIA - potassium chlorate pellet

United States - English - NLM (National Library of Medicine)

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Active ingredient:
POTASSIUM CHLORATE (UNII: H35KS68EE7) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698)
Available from:
Natural Health Supply
INN (International Name):
POTASSIUM CHLORATE
Composition:
POTASSIUM CHLORATE 30 [hp_C] in 1 mL
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Indications: To be used for acute self-limiting conditions according to standard homeopathic indications Purpose: HEMORRHOIDS PROCTALGIA
Authorization status:
unapproved homeopathic
Authorization number:
64117-245-01, 64117-245-02

HEMORRHOIDS PROCTALGIA - potassium chlorate pellet

Natural Health Supply

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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Indications

Indications: To be used for acute self-limiting conditions according to standard homeopathic

indications

Active Ingredient

KALI CHLORICUM

Directions

Take at onset of symptoms. Repeat every 2 hours or as needed until relieved. If condition persists or

worsens discontinue use and consult a practitioner.

Adults: dissolve 5-10 pellets in 1 oz. of filtered water or take dry by mouth. Children and infants: 1-5

pellets.

Keep Out of Reach of Children

Keep these and all medications out of the reach of children.

Warning

If pregnant or nursing, consult a practitioner before using.

Inactive Ingredients

Inactive Ingredients - Lactose, Sucrose

Purpos e

Purpose: HEMORRHOIDS PROCTALGIA

Package Label

Est. No. 1724217

Natural Health Supply

505-474-9175

Homeopathic Medicated Pellets

Do not use if clear bottle seal is broken.Do not use if perforated cap seal is broken.

KALI CHLORICUM 30CC

Lot #__________________

HEMORRHOIDS PROCTALGIA

potassium chlorate pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 4117-245

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of

Stre ng th

Stre ng th

PO TASSIUM CHLO RATE (UNII: H35KS6 8 EE7) (POTASSIUM CATION - UNII:29 5O53K152,

CHLORIDE ION - UNII:Q32ZN48 6 9 8 )

POTASSIUM

CHLORATE

30 [hp_C]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

LACTO SE (UNII: J2B2A4N9 8 G)

SUCRO SE (UNII: C151H8 M554)

Natural Health Supply

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 4117-245-0 1

1.8 75 mL in 1 BOTTLE, GLASS

2

NDC:6 4117-245-0 2

7.5 mL in 1 BOTTLE, GLASS

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 6 /0 4/19 9 8

Labeler -

Natural Health Supply (018504618)

Registrant -

Natural Health Supply (018504618)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Natural Health Supply

0 18 50 46 18

ma nufa c ture

Revised: 7/2011

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