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Doxycycline Tablets and Advanced Acne Wash

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Overview

What is BenzoDox 30 Kit?

Doxycycline tablets, USP is a broad-spectrum antibacterial synthetically derived from oxytetracycline. Doxycycline 100 mg tablets contain doxycycline monohydrate equivalent to 100 mg of doxycycline for oral administration. Inactive ingredients include anhydrous lactose, microcrystalline cellulose, corn starch, colloidal silicon dioxide, magnesium stearate, polyvinyl alcohol, titanium dioxide, polyethylene glycol, talc, D&C yellow #10 aluminum lake, and FD&C yellow #6 aluminum lake. The chemical designation of the light-yellow crystalline powder is 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrate.

Structural formula:

Doxycycline tablets, USP has a high degree of lipid solubility and a low affinity for calcium binding. It is highly stable in normal human serum. Doxycycline will not degrade into an epianhydro form.



What does BenzoDox 30 Kit look like?



What are the available doses of BenzoDox 30 Kit?

Sorry No records found.

What should I talk to my health care provider before I take BenzoDox 30 Kit?

Sorry No records found

How should I use BenzoDox 30 Kit?

Treats and helps prevent acne

Wet face

Apply to hands then work into a lather and massage gently onto face

Rinse thoroughly and pat dry

Because excessive drying of the skin may occur, start with one application daily, then increase to 2 times daily if needed or as directed by a doctor

If bothersome dryness or peeling occurs, reduce usage to once a day or every other day

If going outside, apply sunscreen after using this product.

If irritation or sensitivity develops, stop use of both products and ask a doctor.


What interacts with BenzoDox 30 Kit?

Sorry No Records found


What are the warnings of BenzoDox 30 Kit?

Sorry No Records found


What are the precautions of BenzoDox 30 Kit?

Sorry No Records found


What are the side effects of BenzoDox 30 Kit?

Sorry No records found


What should I look out for while using BenzoDox 30 Kit?

This drug is contraindicated in persons who have shown hypersensitivity to any of the tetracyclines.

For external use only


What might happen if I take too much BenzoDox 30 Kit?

In case of overdosage, discontinue medication, treat symptomatically and institute supportive measures. Dialysis does not alter serum half-life, and it would not be of benefit in treating cases of overdosage.


How should I store and handle BenzoDox 30 Kit?

Store the generator and the eluate, Sodium Pertechnetate Tc99m Injection, below 25°C (77°F). Do not freeze.Store the saline eluent vial below 25°C (77°F). Do not freeze.Storage should be in accordance with local regulations for radioactive materials.Store the generator and the eluate, Sodium Pertechnetate Tc99m Injection, below 25°C (77°F). Do not freeze.Store the saline eluent vial below 25°C (77°F). Do not freeze.Storage should be in accordance with local regulations for radioactive materials.Store the generator and the eluate, Sodium Pertechnetate Tc99m Injection, below 25°C (77°F). Do not freeze.Store the saline eluent vial below 25°C (77°F). Do not freeze.Storage should be in accordance with local regulations for radioactive materials.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.Doxycycline Tablets, USP 100 mg are yellow, film coated, caplets, debossed LCI on one face and 1338 on the other face. Each tablet contains doxycycline monohydrate equivalent to 100 mg of doxycycline.They are supplied as follows:Bottles of 30 NDC 42783-601-30Bottles of 60 NDC 42783-601-60Dispense in a tight light-resistant container with a child-resistant closure.Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].PROTECT FROM LIGHT.


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Tetracyclines are readily absorbed and are bound to plasma proteins in varying degrees. They are concentrated by the liver in the bile and excreted in the urine and feces at high concentrations in a biologically active form. Doxycycline is virtually completely absorbed after oral administration.

Following a 200 mg dose of doxycycline monohydrate, 24 normal adult volunteers averaged the following serum concentration values:

Excretion of doxycycline by the kidney is about 40%/72 hours in individuals with normal function (creatinine clearance about 75 mL/min). This percentage excretion may fall as low as 1-5%/72 hours in individuals with severe renal insufficiency (creatinine clearance below 10 mL/min). Studies have shown no significant difference in serum half-life of doxycycline (range 18-22 hours) in individuals with normal and severely impaired renal function.

Hemodialysis does not alter serum half-life.

Non-Clinical Toxicology
This drug is contraindicated in persons who have shown hypersensitivity to any of the tetracyclines.

For external use only

Because tetracyclines have been shown to depress plasma prothrombin activity, patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage.

Since bacteriostatic drugs may interfere with the bactericidal action of penicillin, it is advisable to avoid giving tetracyclines in conjunction with penicillin.

Absorption of tetracyclines is impaired by antacids containing aluminum, calcium, or magnesium, and iron-containing preparations.

Barbiturates, carbamazepine, and phenytoin decrease the half-life of doxycycline.

The concurrent use of tetracycline and methoxyflurane has been reported to result in fatal renal toxicity.

Concurrent use of tetracycline may render oral contraceptives less effective.

PRECAUTIONS

Due to oral doxycycline's virtually complete absorption, side effects to the lower bowel, particularly diarrhea, have been infrequent. The following adverse reactions have been observed in patients receiving tetracyclines.

Gastrointestinal

DOSAGE AND ADMINISTRATION

Skin

WARNINGS

Renal Toxicity

WARNINGS

Hypersensitivity Reaction

Blood

Other

PRECAUTIONS – Genera

When given over prolonged periods, tetracyclines have been reported to produce brown-black microscopic discoloration of the thyroid gland. No abnormalities of thyroid function are known to occur.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

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