CUPRUM STANNUM liquid

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Aktīvā sastāvdaļa:

NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4), SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF), TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5), COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5), POTASSIUM ALUM (UNII: 1L24V9R23S) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)

Pieejams no:

Uriel Pharmacy Inc.

SNN (starptautisko nepatentēto nosaukumu):

NITRIC ACID

Kompozīcija:

NITRIC ACID 2 [hp_X] in 1 mL

Ievadīšanas:

ORAL

Receptes veids:

OTC DRUG

Ārstēšanas norādes:

Directions: FOR ORAL USE ONLY. Use: Temporary relief of digestive upset.

Autorizācija statuss:

unapproved homeopathic

Produkta apraksts

CUPRUM STANNUM- CUPRUM STANNUM 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._
----------
CUPRUM STANNUM
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 Ingredients: 100gm contains: 94gm Acidum nitricum (Nitric acid)
2X, 40gm
Acidum sulfuricum (Sulfuric acid) 2X, 20gm Stannum met. (Metallic tin)
2X, 2gm Cuprum
met. (Copper) 3X; Alumen (Potassium aluminum sulfate) 3X
Inactive Ingredients: Distilled water, Silica
Use: Temporary relief of digestive upset.
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.
Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI
53120
shopuriel.com
CUPRUM STANNUM
cuprum stannum liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-3145
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4)
NITRIC ACID
2 [hp_X]
in 1 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)
SULFURIC ACID
2 [hp_X]
in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)
TIN
2 [hp_X]
in 1 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)
COPPER
3 [hp_X]
in 1 mL
POTASSIUM ALUM (UNII: 1L24V9R23S) (ALUMINUM HYDROXIDE -
UNII:5QB0T2IUN0)
POTASSIUM ALUM
3 [hp_X]
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PRODUCT CHARACTERISTICS
COLOR
white
SCORE
SHAPE
SIZE
FLAVOR
IMPRINT CODE
CONTAINS
PACKAGIN