KALIUM CARBONICUM 12 SPECIAL ORDER- kalium carbonicum 12 special order 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.

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Kalium carbonicum 12 Special Order

Directions: FOR ORAL USE ONLY.

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

Active Ingredient: Kalium carbonicum 12X

Inactive Ingredient: Distilled water

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. 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.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.

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

KaliumCarbonicum12SOLiquid

KALIUM CARBONICUM 12 SPECIAL ORDER 
kalium carbonicum 12 special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6067
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE12 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-6067-360 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-6067)

Revised: 4/2018
Document Id: 6ad48609-b121-ecf3-e053-2991aa0ad704
Set id: 6014aa18-baab-4fa9-987f-4f28a545600a
Version: 2
Effective Time: 20180427
 
Uriel Pharmacy Inc.