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Rondec

Indications & Dosage
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INDICATIONS

For symptomatic relief of seasonal and perennial allergic rhinitis and vasomotor rhinitis.

Rondec Oral Drops, Rondec Syrup and Rondec Tablet are immediate release dosage forms allowing titration of dose up to four times a day.

Rondec-TR Tablet utilizes a gradual release mechanism providing approximately a 12 hour therapeutic effect, thus allowing twice daily dosage.

DOSAGE AND ADMINISTRATION

AGE
DOSE
FREQUENCY*
Rondec Oral Drops for oral use only
1-3 months ¼ dropperful (¼ mL)
3-6 months ½ dropperful (½ mL)
q.i.d.
6-9 months ¾ dropperful (¾ mL)
q.i.d.
9-18 months 1dropperful (1mL)
q.i.d.
Rondec Syrup and Rondec Tablet
18months - 6years ½ teaspoonful (2.5 mL)
q.i.d.
adults and pediatric patients 6 years and over 1 teasponful (5 mL)
or
1 tablet
q.i.d.
Rondec-TR Tablet
adults and adolescents 12 years and over 1tablet
b.i.d

*In mild cases or in particularly sensitive patients, less frequent or reduced doses may be adequate.

HOW SUPPLIED

Rondec Oral Drops, berry-flavored

in 30 mL bottles for dropper dosage

NDC 51479-020-03
Calibrated shatterproof dropper enclosed in each carton. Container meets safety closure requirements.

 

Rondec Syrup, berry-flavored

in 16-fl-oz (1-pint) bottles

NDC 51479-021-48

and 4 fl-oz bottles

NDC 51479-021-12
Dispense in USP tight glass container.

 

Rondec Tablet

in bottles of 100

NDC 51479-022-01

and bottles of 500

NDC 51479-022-05
Each orange-colored tablet marked with R and the number 5726 for professional identification. Dispense in USP tight container.

 

Rondec TR Tablet

in bottles of 100

NDC 51479-025-01
Each blue colored tablet marked with R and the number 6240 for professional identification. Dispense in USP tight container.

Recommended storage: Store below 86° F (30° C).

CAUTION: Federal (U.S.A.) law prohibits dispensing without prescription.

Brand Name: Rondec
Generic Name: Carbinoxamine Maleate and Pseudoephedrine HCl

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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