encer

Manufacturer
B'OKCARES LTD
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:36:29

Label at a glance#

Productencer
Active ingredientCADMIUM SULFIDE, CARBO ANIMALIS, PHOSPHORIC ACID, RADIUM BROMIDE, ALCOHOL, X-RAY EXPOSED (1000 RAD)
Label structure9 sections

Indications and uses

Temporarily relieves symptoms of fatigue caused by radiation and\ or radiotherapy.

Dosage and administration

Chew one tablet and allow to dissolve in the mouth for 1 minute before swallowing. Repeat 6 hours after the first dose. Must not be taken 10 minutes before or after eating. • Must not be taken within 6 hours of bedtime. • Do not exceed usage directions. May be taken during radiotherapy and for 12 weeks after the end of radiation treatment. Use may be continued for as long as fatigue related to radiation lasts.

Storage and handling

• Do not use if blister is broken. • Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Cadmium sulphuratum 30C HPUS*

Carbo animalis 30C HPUS*

Phosphoricum acidum 30C HPUS*

Radium bromatum 30C HPUS*

X-Ray 6C HPUS*

* The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopoeia of the Unites States.

Purpose

OTC - PURPOSE SECTION

Cadmium sulphuratum 30C HPUS* .... Relieves fatigue symptoms

Carbo animalis 30C HPUS* .... Relieves fatigue symptoms

Phosphoricum acidum 30C HPUS* .... For poor concentration

Radium bromatum 30C HPUS* .... Relieves radiation fatigue

X-Ray 6C HPUS* .... Relieves radiation fatigue

* The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopoeia of the Unites States.

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves symptoms of fatigue caused by radiation and\ or radiotherapy.

Warnings

WARNINGS SECTION

Warnings

OTC - WHEN USING SECTION

When using this product

  • over-arousal, restlessness, or difficulty falling asleep may occur. Reduce use to one dose in the morning if this occurs.

OTC - STOP USE SECTION

Stop use and ask doctor if

  • condition worsens
  • there is no improvement

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you are taking a prescription drug or have a serious medical condition.

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. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Chew one tablet and allow to dissolve in the mouth for 1 minute before swallowing. Repeat 6 hours after the first dose.

  • Must not be taken 10 minutes before or after eating. • Must not be taken within 6 hours of bedtime. • Do not exceed usage directions. May be taken during radiotherapy and for 12 weeks after the end of radiation treatment. Use may be continued for as long as fatigue related to radiation lasts.

Other information

STORAGE AND HANDLING SECTION

• Do not use if blister is broken. • Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Magnesium stearate, maltodextrin, sucrose.

Questions or Comments?

OTC - QUESTIONS SECTION

Questions or comments?

Encer.life

Tel: +1 319 895 1720

Email: sales@Encer.life

B'OKCARES LTD.

Distributed by HC Supplement Solutions LLC

838 Walker Rd Ste 21-2 Dover, DE

19904, USA.

Made in USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 82509-001-60

Homeopathic

Fatigue symptoms relief

300 mg each

60 TABLETS

11

OTC - PURPOSE SECTION

Temporarily relieves symptoms of fatigue cause by radiation and\ or radiotherapy.

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

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82509-00182509-001-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
encerCADMIUM SULPHURATUM, CARBO ANIMALIS, PHOSPHORICUM ACIDUM, RADIUM BROMATUM, X-RAYB'OKCARES LTD5d7bce73-077c-41c5-9b6b-8580dc79dc402025-12-29WarningsExact identifier
ndc (package): 82509-001-60
ndc (product): 82509-001
ndc11 (package): 82509000160
spl id: 471e8d51-2f64-73af-e063-6394a90a18cb
spl set id: 5d7bce73-077c-41c5-9b6b-8580dc79dc40

Reported adverse events (FAERS/openFDA)#

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