Rynex Pe

BROMPHENIRAMINE MALEATE and Phenylephrine HCL · Liquid · Oral

Over the counter alpha-1 Adrenergic Agonist

Active ingredient

Active Ingredients (in each 5 nil teaspoonful) Purpose Brompheniramine Maleate 1 mg Antihistamine Phenylephrine HCl 2.5 mg Nasal Decongestant

Purpose

Active Ingredients (in each 5 nil teaspoonful) Purpose Brompheniramine Maleate 1 mg Antihistamine Phenylephrine HCl 2.5 mg Nasal Decongestant

Uses

Uses temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes nasal congestion reduces swelling of nasal passage

Warnings

Warnings Do not exceed recommended dosage. Do not take this product if you are now taking a prescription monoamine oxidase inhibitor (MA0I) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma heart disease high blood pressure thyroid disease diabetes mellitus difficulty in urination due to enlargement of the prostate gland Ask a doctor before use if you are taking sedatives or tranquilizers. When using this product excitability may occur, especially in children may cause drowsiness sedalives and tranquilizers may increase drowsiness effect avoid alcoholic beverages use caution when driving a motor vehicle or operating machinery Stop use and ask doctor if nervousness, dizziness, or sleeplessness occur If symptoms do not improve within 7 days or are accompanied by fever, consult a doctor new symptoms occur If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Do not use

Do not take this product if you are now taking a prescription monoamine oxidase inhibitor (MA0I) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use

Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma heart disease high blood pressure thyroid disease diabetes mellitus difficulty in urination due to enlargement of the prostate gland Ask a doctor before use if you are taking sedatives or tranquilizers.

When using this product

When using this product excitability may occur, especially in children may cause drowsiness sedalives and tranquilizers may increase drowsiness effect avoid alcoholic beverages use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor

Stop use and ask doctor if nervousness, dizziness, or sleeplessness occur If symptoms do not improve within 7 days or are accompanied by fever, consult a doctor new symptoms occur

Pregnancy or breast-feeding

If pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children. In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Directions

Directions Do not exceed recommended dosage. Adults and children 12 years of age and over: 4 teaspoonfuls (20 mL) every 4 hours, not to exceed 24 teaspoonfuls in 24 hours, or as directed by a doctor. Children 6 to under 12 years of age: 2 teaspoonfuls(10 mL) every 4 hours, not to exceed 1 teaspoonfuls in 24 hours, or as directed by a doctor. Children under 6 years of age: Consult a doctor

Other information

Other information Store at 59° - 86° F (15° - 30° C) [see USP for Controlled Room Temperature].

Inactive ingredients

Inactive ingredients Bubblegum Flavor, Citric Acid, FD&C Red #40, Methyl Paraben, Potassium Citrate, Potassium Sorbate, Propyl Paraben, Propylene Glycol, Purified Water, Sorbitol Solution 70%, Sucralose.

Questions?

Questions Comments? Call 1-800-543-9560

Label text from the FDA structured product label by EDWARDS PHARMACEUTICALS, INC. (revised Mar 5, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Rynex Pe NDC products (1)

NDCStrength & formLabelerType
0485-0202Brompheniramine Maleate 1 mg/5mL; Phenylephrine Hydrochloride 2.5 mg/5mL
Liquid
EDWARDS PHARMACEUTICALS, INC.OTC MONOGRAPH DRUG

Frequently asked questions

What is Rynex Pe used for?

Uses temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes nasal congestion reduces swelling of nasal passage

Who makes Rynex Pe?

Rynex Pe is listed by 1 labeler in the FDA NDC directory, including EDWARDS PHARMACEUTICALS, INC..