Dye Free Wal Dryl Allergy Childrens
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Questions & Answers
Side Effects & Adverse Reactions
- with any other product containing diphenhydramine, even one used on skin
- to make a child sleepy
- a breathing problem such as chronic bronchitis
- glaucoma
- a sodium-restricted diet
taking sedatives or tranquilizers
- marked drowsiness may occur
- sedatives and tranquilizers may increase drowsiness
- excitability may occur, especially in children
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
- with any other product containing diphenhydramine, even one used on skin
- to make a child sleepy
- a breathing problem such as chronic bronchitis
- glaucoma
- a sodium-restricted diet
taking sedatives or tranquilizers
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- sneezing
- runny nose
- itchy, watery eyes
- itching of the nose or throat
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Dye Free Wal Dryl Allergy Childrens Manufacturers
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Walgreens
![Dye Free Wal Dryl Allergy Childrens (Diphenhydramine Hydrochloride) Liquid [Walgreens]](/wp-content/themes/bootstrap/assets/img/loading2.gif)
Dye Free Wal Dryl Allergy Childrens | American Health Packaging
Optimal dosage should be established by individual titration of the components (see boxed Warning).
Edema in adults (congestive heart failure, hepatic cirrhosis, or nephrotic syndrome). The usual maintenance dose of spironolactone and hydrochlorothiazide tablets is 100 mg each of spironolactone and hydrochlorothiazide daily, administered in a single dose or in divided doses, but may range from 25 mg to 200 mg of each component daily depending on the response to the initial titration. In some instances it may be desirable to administer separate tablets of either spironolactone or hydrochlorothiazide in addition to spironolactone and hydrochlorothiazide tablets in order to provide optimal individual therapy.
The onset of diuresis with spironolactone and hydrochlorothiazide tablets occurs promptly and, due to prolonged effect of the spironolactone component, persists for two to three days after spironolactone and hydrochlorothiazide tablets are discontinued.
Essential hypertension. Although the dosage will vary depending on the results of titration of the individual ingredients, many patients will be found to have an optimal response to 50 mg to 100 mg each of spironolactone and hydrochlorothiazide daily, given in a single dose or in divided doses.
Concurrent potassium supplementation is not recommended when spironolactone and hydrochlorothiazide tablets are used in the long-term management of hypertension or in the treatment of most edematous conditions, since the spironolactone content of spironolactone and hydrochlorothiazide tablets is usually sufficient to minimize loss induced by the hydrochlorothiazide component.
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