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Calcium citrate, Iron pentacarbonyl, Cholecalciferol, .Alpha.-Tocopherol, Dl-, Pyridoxine hydrochloride, Folic Acid, Docusate Sodium, and Doconexent

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Overview

What is CitraNatal Harmony 3.0?

CitraNatal Harmony is a prescription prenatal/postnatal multivitamin/mineral soft gelatin capsule. The prenatal vitamin is a purple, opaque soft gelatin capsule containing a greenish-gray liquid to semi-solid fill. The capsule is printed “0796” in white ink.



What does CitraNatal Harmony 3.0 look like?



What are the available doses of CitraNatal Harmony 3.0?

Sorry No records found.

What should I talk to my health care provider before I take CitraNatal Harmony 3.0?

Sorry No records found

How should I use CitraNatal Harmony 3.0?

CitraNatal Harmony is a multivitamin/mineral prescription drug indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers.

One capsule daily or as directed by a physician.

Store at controlled room temperature.

NOTICE

Contact with moisture can discolor or erode the capsule.


What interacts with CitraNatal Harmony 3.0?

This product is contraindictated in patients with a known hypersensitivity to any of the ingredients.



What are the warnings of CitraNatal Harmony 3.0?

Sorry No Records found


What are the precautions of CitraNatal Harmony 3.0?

Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.


What are the side effects of CitraNatal Harmony 3.0?

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

CAUTION

Exercise caution to ensure that the prescribed dosage of DHA does not exceed 1 gram (1000 mg) per day.


What should I look out for while using CitraNatal Harmony 3.0?

This product is contraindictated in patients with a known hypersensitivity to any of the ingredients.

Ingestion of more than 3 grams of omega-3 fatty acids per day has been shown to have potential antithrombotic effects, including an increased bleeding time and INR. Administration of omega-3 fatty acids should be avoided in patients on anticoagulants and in those known to have an inherited or acquired bleeding diathesis.

WARNING

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where vitamin B is deficient.


What might happen if I take too much CitraNatal Harmony 3.0?

Sorry No Records found


How should I store and handle CitraNatal Harmony 3.0?

Storage and HandlingBottles of 30 capsules each - NDC 0178-0796-30To report a serious adverse event or obtain product information, call (210) 696-8400Please consult your health care provider with any dietary concerns.Manufactured for: MISSION PHARMACAL COMPANY San Antonio, TX USA 78230 1355 Bottles of 30 capsules each - NDC 0178-0796-30To report a serious adverse event or obtain product information, call (210) 696-8400Please consult your health care provider with any dietary concerns.Manufactured for: MISSION PHARMACAL COMPANY San Antonio, TX USA 78230 1355 Bottles of 30 capsules each - NDC 0178-0796-30To report a serious adverse event or obtain product information, call (210) 696-8400Please consult your health care provider with any dietary concerns.Manufactured for: MISSION PHARMACAL COMPANY San Antonio, TX USA 78230 1355 Bottles of 30 capsules each - NDC 0178-0796-30To report a serious adverse event or obtain product information, call (210) 696-8400Please consult your health care provider with any dietary concerns.Manufactured for: MISSION PHARMACAL COMPANY San Antonio, TX USA 78230 1355


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
This product is contraindictated in patients with a known hypersensitivity to any of the ingredients.

Ingestion of more than 3 grams of omega-3 fatty acids per day has been shown to have potential antithrombotic effects, including an increased bleeding time and INR. Administration of omega-3 fatty acids should be avoided in patients on anticoagulants and in those known to have an inherited or acquired bleeding diathesis.

WARNING

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where vitamin B is deficient.

The CNS effects of butalbital may be enhanced by monoamine oxidase (MAO) inhibitors.

Butalbital and acetaminophen may enhance the effects of: other narcotic analgesics, alcohol, general anesthetics, tranquilizers such as chlordiazepoxide, sedative-hypnotics, or other CNS depressants, causing increased CNS depression.

Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

CAUTION

Exercise caution to ensure that the prescribed dosage of DHA does not exceed 1 gram (1000 mg) per day.

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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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