encer

Product NDC
82509-001
11-digit product format
825090001
Labeler code
82509
Product ID
82509-001_471e8d51-2f64-73af-e063-6394a90a18cb
Type
HUMAN OTC DRUG
Nonproprietary name
Cadmium sulphuratum, Carbo animalis, Phosphoricum acidum, Radium bromatum, X-ray
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
B'OKCARES LTD
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-05-22
Substance
ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM SULFIDE; CARBO ANIMALIS; PHOSPHORIC ACID; RADIUM BROMIDE
Active strength
6; 30; 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
encer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CADMIUM SULFIDE6 [hp_C]/1
CARBO ANIMALIS30 [hp_C]/1
PHOSPHORIC ACID30 [hp_C]/1
RADIUM BROMIDE30 [hp_C]/1
ALCOHOL, X-RAY EXPOSED (1000 RAD)30 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
057EZR4Z7QInternal UNII lookup
279O8I0433Internal UNII lookup
E4GA8884NNInternal UNII lookup
R74O7T8569Internal UNII lookup
6PRJ93602PInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5d7bce73-077c-41c5-9b6b-8580dc79dc40Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82509-001-60encer20 in 1 BLISTER PACKTABLET, ORALLY DISINTEGRATING203
82509-001-60encer3 in 1 CARTONTABLET, ORALLY DISINTEGRATING33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82509-001ENCER (CADMIUM SULPHURATUM, CARBO ANIMALIS, PHOSPHORICUM ACIDUM, RADIUM BROMATUM, X-RAY) TABLET, ORALLY DISINTEGRATING [B'OKCARES LTD]2Current NDC, 2 package rows20241017_5d7bce73-077c-41c5-9b6b-8580dc79dc40.zip

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
encerCADMIUM SULPHURATUM, CARBO ANIMALIS, PHOSPHORICUM ACIDUM, RADIUM BROMATUM, X-RAYB'OKCARES LTD5d7bce73-077c-41c5-9b6b-8580dc79dc402025-12-29WarningsExact identifier
ndc (product): 82509-001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82509-001-60825090001603 BLISTER PACK in 1 CARTON (82509-001-60) / 20 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK3 blister pack2023-05-22NoNoCurrent