KALIUM ACETICUM COMP. 6 powder

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM RUBRUM EXOSKELETON - UNII:2CA71K0DLE), SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ), POTASSIUM ACETATE (UNII: M911911U02) (POTASSIUM CATION - UNII:295O53K152), ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)

Available from:

Uriel Pharmacy Inc.

INN (International Name):

CORALLIUM RUBRUM EXOSKELETON

Composition:

CORALLIUM RUBRUM EXOSKELETON 6 [hp_X] in 1 g

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE ONLY. Use: Temporary relief of skin rash.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

KALIUM ACETICUM COMP. 6- KALIUM ACETICUM COMP. 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._
----------
KALIUM ACETICUM COMP. 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 Ingredients: Antimonite (Nat. antimony trisulfide) 6X,
Corallium rubrum (Red coral)
6X, Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate) 6X
Inactive Ingredient: Lactose
"prepared using rhythmical processes"
Use: Temporary relief of skin rash.
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 shopuriel.com
KALIUM ACETICUM COMP. 6
kalium aceticum comp. 6 powder
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-6004
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH STRENGTH
Uriel Pharmacy Inc.
CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM
RUBRUM EXOSKELETON - UNII:2CA71K0DLE)
CORALLIUM RUBRUM
EXOSKELETON
6 [hp_X]
in 1 g
SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ)
SAFFRON
6 [hp_X]
in 1 g
POTASSIUM ACETATE (UNII: M911911U02) (POTASSIUM CATION -
UNII:295O53K152)
POTASSIUM ACETATE
6 [hp_X]
in 1 g
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE -
UNII:F79059A38U)
ANTIMONY TRISULFIDE
6 [hp_X]
in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
LACTOSE (UNII: J2B2A4N98G)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:48