About the medicine

How to use Ceel

INFORMATION PLACED ON OUTER PACKAGING

CONTAINER

1. NAME OF THE MEDICINAL PRODUCT

CEEL

50 mg + 100 mg, coated tablets
Acidum ascorbicum + int-rac-α-Tocopherylis acetas

2. CONTENT OF ACTIVE SUBSTANCES

Composition:

1 tablet contains:

  • active substances: 50 mg of ascorbic acid (vitamin C) and 100 mg of all- rac- α-tocopheryl acetate (vitamin E).

3. LIST OF EXCIPIENTS

Excipients: povidone K 25, cellulose, magnesium stearate, instant sorbitol.
Coating composition: lactose monohydrate, hypromellose, triacetin, yellow iron oxide (E 172), titanium dioxide (E 171), quinoline yellow (E 104).

4. PHARMACEUTICAL FORM AND CONTENT OF THE PACKAGING

50 tablets

EAN.UCC Code: 5909990892464

60 tablets

EAN.UCC Code: 5909990892471

5. METHOD AND ROUTE OF ADMINISTRATION

Method of administration and route of administration:oral administration. Children over 12 years of age and adults: 1 to 2 tablets per day. Children under 12 years of age: as directed by a doctor.

6. WARNING ABOUT STORAGE OF THE MEDICINAL PRODUCT IN A PLACE INACCESSIBLE TO CHILDREN

IN A PLACE INVISIBLE AND INACCESSIBLE TO CHILDREN

Store in a place inaccessible to children.

7. OTHER SPECIAL WARNINGS, IF NECESSARY

NOTE: A DESICCANT IS PLACED UNDER THE CLOSURE.

Contraindications:

  • hypersensitivity to the components of the preparation;
  • vitamin K deficiency (possibility of bleeding);
  • disorders of intestinal absorption.

Precautions:use with caution in patients with a history of kidney stones, gout, cystinuria, glucose-6-phosphate dehydrogenase deficiency, hemochromatosis, thalassemia, sideroblastic anemia. During long-term concurrent administration of the drug and oral anticoagulant drugs due to the possibility of hypoprothrombinemia.
Do not exceed the recommended dosage without consulting a doctor.
If the patient has previously been diagnosed with intolerance to certain sugars, the patient should consult a doctor before taking the drug.
The drug may cause allergic reactions.
Pregnancy. Breastfeeding:consult a doctor before use.
Driving and operating machinery:the drug does not affect psychophysical fitness.
Interactions:vitamin E may enhance the effect of anticoagulant drugs. Cholestyramine and colestipol may reduce the effectiveness of the drug. Vitamin E used concurrently with iron preparations may weaken their effect, especially in children with iron deficiency anemia.

8. EXPIRY DATE

Expiry date:

9. STORAGE CONDITIONS

Store at a temperature below 25°C.

10. SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED MEDICINAL PRODUCT OR WASTE DERIVED FROM IT, IF APPROPRIATE

UNUSED MEDICINAL PRODUCT OR WASTE DERIVED FROM IT, IF APPROPRIATE

11. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER

Marketing authorisation holder:

PPF "GEMI" Grzegorz Nowakowski
ul. Mickiewicza 36
05-480 Karczew

12. MARKETING AUTHORISATION NUMBER

Marketing authorisation number: 10624

13. BATCH NUMBER

Batch number:

14. GENERAL CATEGORY OF AVAILABILITY

Medicinal product available without a prescription – OTC.

15. INSTRUCTIONS FOR USE

Indications for use:

  • treatment of vitamin C and E deficiency;
  • supporting treatment of myocardial infarction, coronary heart disease;
  • in diseases related to oxidative stress.

16. INFORMATION PROVIDED IN BRAILLE

ceel

17. OTHER INFORMATION

Effect:

The combination of vitamins C and E allows for the use of their synergistic effect and the protective effect of vitamin C on vitamin E. Vitamin E protects against oxidation of other vitamins, especially vitamin A, as well as hormones and enzymes. It prevents excessive oxidation of lipids and unsaturated fatty acids, thus acting protectively on body cells. It also models the biosynthesis of prostaglandins and platelet aggregation. It is also attributed an important role in protecting the body against the harmful effects of free radicals and lipid peroxides.
Vitamin C is a compound necessary in redox processes, in the synthesis of catecholamines and other metabolic changes occurring in body cells.
C may have a supporting effect in the treatment of patients with elevated LDL cholesterol levels, especially after myocardial infarction.
Undesirable effects:tolerance to vitamin E is good. After exceeding the recommended doses, the following may occur: feeling of fatigue, weakness, headaches, nausea, diarrhea, bloating, rash. Vitamin C occurs in the CEEL drug in a dose twice lower than the recommended daily intake and therefore undesirable effects related to its content are unlikely.
If any undesirable effects occur, including any undesirable effects not listed in this packaging, you should inform your doctor, pharmacist, or nurse. Undesirable effects can be reported directly to the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
e-mail: ndl@urpl.gov.pl.
Thanks to the reporting of undesirable effects, more information can be collected on the safety of the drug.

MINIMUM INFORMATION ON SMALL OUTER PACKAGING

BLISTER

1. NAME OF THE MEDICINAL PRODUCT AND ROUTE OF ADMINISTRATION

CEEL

50 mg + 100 mg, coated tablets
Acidum ascorbicum + int-rac-α-Tocopherylis acetas

2. METHOD OF ADMINISTRATION

3. EXPIRY DATE

4. BATCH NUMBER, DONATION CODES, AND PRODUCT CODES

Batch number and expiry date:on the weld

5. CONTENT OF THE PACKAGING WITH ADMINISTRATION OF MASS, VOLUME, OR NUMBER OF UNITS

UNITS

6. OTHER

PPF "GEMI" Grzegorz Nowakowski
ul. Mickiewicza 36, 05-480 Karczew

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