FDA.reportPublic FDA data

Cadmium sulphuratum

Manufacturer
Boiron | Boiron, Inc.
Effective date
2024-04-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:38

Label at a glance#

ProductCadmium sulphuratum
Active ingredientCADMIUM SULFIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Cadmium sulphuratum 200CK HPUS

Less than 10 -12 mg cadmium per pellet

Active ingredient**: See product name on front panel (**contains 0.443 mg of the active ingredient per pellet).

INDICATIONS & USAGE SECTION

Uses: See symptoms on front panel.

Relieves acid indigestion with nausea and cold sweats *

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

BoironUSA.com Info@boiron.com
1-800-BOIRON-1 (1-800-264-7661)
Distributed by Boiron, Inc.
Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

Do not use if pellet dispenser seal is broken.
Contains approx.80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-1015-41Cadmium sulphuratum200 [kp_C] in 1 TUBEPELLET2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-1015CADMIUM SULPHURATUM (CADMIUM SULFIDE) PELLET [BOIRON]2Current NDC, 1 package rows20240418_163a22a1-1903-5dc5-e063-6394a90aa2e2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-10150220-1015-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
CADMIUM SULFIDE057EZR4Z7QACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cadmium sulphuratumCADMIUM SULFIDEBoiron163a22a1-1903-5dc5-e063-6394a90aa2e22024-04-16Exact identifier
ndc (package): 0220-1015-41
ndc (product): 0220-1015
ndc11 (package): 00220101541
spl id: 163aef1f-24b7-9d0c-e063-6394a90a98de
spl set id: 163a22a1-1903-5dc5-e063-6394a90aa2e2

Reported adverse events (FAERS/openFDA)#

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