KALIUM ACETICUM COMP 6 pellet

দেশ: মার্কিন যুক্তরাষ্ট্র

ভাষা: ইংরেজি

সূত্র: NLM (National Library of Medicine)

সক্রিয় উপাদান:

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

থেকে পাওয়া:

Uriel Pharmacy Inc.

প্রশাসন রুট:

ORAL

প্রেসক্রিপশন টাইপ:

OTC DRUG

থেরাপিউটিক ইঙ্গিত:

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

অনুমোদন অবস্থা:

unapproved homeopathic

পণ্য বৈশিষ্ট্য

KALIUM ACETICUM COMP 6- KALIUM ACETICUM COMP 6 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._
----------
KALIUM ACETICUM COMP 6X
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 (Nat. antimony trisulfide) 6X, Corallium
rubrum (Red coral)
6X, Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate) 6X
Inactive Ingredient: Organic sucrose
"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. Contains sugar. Diabetics and persons
intolerant of
sucrose (sugar): Consult a doctor before use. Contains traces of
lactose. 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
shopuriel.com Lot:
KALIUM ACETICUM COMP 6
kalium aceticum comp 6 pellet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-6079
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ)
SAFFRON
6 [hp_X]
POTASSIUM ACETATE (UNII: M911911U02) (POTASSIUM CATION -
UNII:295O53K152)
POTASSIUM ACETATE
6 [hp_X]
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]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SUCRO