Chamomilla Malachite Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-05-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:54:38

Label at a glance#

ProductChamomilla Malachite Special Order

Active ingredientCORALLIUM RUBRUM EXOSKELETON, SAFFRON, CUPRIC CARBONATE, TOBACCO LEAF, MATRICARIA RECUTITA, ANTIMONY TRISULFIDE, POTASSIUM ACETATE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Chamomilla (Chamomile) 3X, Antimonite (Nat. antimony trisulfide) 6X, Corallium rubrum (Red coral) 6X, Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate) 6X, Malachite (Nat. Copper carbonate) 8X, Nicotiana (Tobacco) 10X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Lactose

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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. Contains traces of lactose. If pregnant or nursing, consult a doctor before use.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ChamomillaMalachiteSOAmpules

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Chamomilla Malachite Special Order
CORALLIUM RUBRUM EXOSKELETON
SAFFRON
CUPRIC CARBONATE
CUPRIC CATION
TOBACCO LEAF
MATRICARIA RECUTITA
ANTIMONY TRISULFIDE
POTASSIUM ACETATE
POTASSIUM CATION
WATER
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-3217	48951-3217-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CORALLIUM RUBRUM EXOSKELETON	2CA71K0DLE	ACTIB
SAFFRON	E849G4X5YJ	ACTIB
CUPRIC CARBONATE	9AOA5F11GJ	ACTIM
TOBACCO LEAF	6YR2608RSU	ACTIB
MATRICARIA RECUTITA	G0R4UBI2ZZ	ACTIB
ANTIMONY TRISULFIDE	F79059A38U	ACTIB
POTASSIUM ACETATE	M911911U02	ACTIB
WATER	059QF0KO0R	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c4475244-bad3-13da-e053-2a95a90a79b3			6c571f10-c5e8-5df1-e053-2a91aa0ad0c7	2021-06-08	Warnings	Exact identifier spl set id: 6c571f10-c5e8-5df1-e053-2a91aa0ad0c7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.