KALI ACETICUM COMP 6 SPECIAL ORDER- kali aceticum comp 6 special order pellet
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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Kalium aceticum comp 6 Special Order

Directions: FOR ORAL USE ONLY.

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

Active Ingredient: Antimonite 6X, Corallium rubrum 6X, Crocus sativa 6X, Kalium aceticum 6X

Inactive Ingredient: Organic sucrose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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 Uriel, East Troy, WI 53120 www.urielpharmacy.com

KaliumAceticumComp6SOPellets

KALI ACETICUM COMP 6 SPECIAL ORDER
kali aceticum comp 6 special order pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-6056
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	6 [hp_X]
CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (CORALLIUM RUBRUM EXOSKELETON - UNII:2CA71K0DLE)	CORALLIUM RUBRUM EXOSKELETON	6 [hp_X]
SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ)	SAFFRON	6 [hp_X]
POTASSIUM ACETATE (UNII: M911911U02) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM ACETATE	6 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	3mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-6056-2	1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009	10/07/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	10/07/2020

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-6056)

Revised: 6/2021

Document Id: c4e8507a-4a4b-8235-e053-2a95a90aa078

Set id: 6fa20cca-31fa-47e1-96e6-3ae8dde85f19

Version: 3

Effective Time: 20210616

Uriel Pharmacy Inc.