to socialize Entre-B Generic Name: brompheniramine maleate and phenylephrine hydrochloride Dosage Form: oral suspension Side Effects Dosage Professional Interactions Pregnancy More User Reviews Support Group Q & A Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here. Entre-B SUSPENSION 4 FL OZ (118 ML) Entre-B NDC 42192-513-04 Suspension Antihistimine Decongestant Bubblegum Flavor Each 5 mL (teaspoonful) contains: Brompheniramine Maleate.............6mg Phenylephrine HCL.......................10mg Rx Only Shake Well DOSAGE AND ADMINISTRATION: Adults and children over 12 years of age: 1 - 2 teaspoonfuls every 12 hours. Children 6 to under 12 years of age: 1 teaspoonful every 12 hours. Children under 6 years of age: Consult a physician. Dispense in a well closed, light-resistant container. Store at controlled room temperature, 20 - 25 C (68 - 77 F) [See USP]. Shake well before use. WARNING: KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY. MANUFACTURED FOR: Acella Pharmaceuticals, LLC 9005 Westside Parkway Alpharetta, GA 30009 Utilizing Neuvosyn Technology Entre-B Suspension Rx Only Entre-B is an antihistamine/nasal decongestant combination for oral administration as a suspension. Each 5 mL (one teaspoonful) of the bubble-gum flavored, suspension for oral administration contains: Phenylephrine HCl .............................. 10 mg Brompheniramine Maleate .................... 6 mg INACTIVE INGREDIENTS: Propylene Glycol, Glycerin, Xanthan Gum, Bubble Gum Flavor, Saccharin Sodium, Sodium Citrate, Citric Acid, Tannic Acid, Magnesium Aluminum Silicate, Natural Masking Flavor, Pink Dye, Benzoic Acid, Methyl Paraben, Propyl Paraben, and Purified Water CLINICAL PHARMACOLOGY Entre-B combines the sympathomimetic decongestant effect of Phenylephrine with the antihistaminic action of Brompheniramine. Phenylephrine: Phenylephrine is a decongestant which is a potent postsynaptic receptor agonist with little effect on receptors of the heart. A direct action at receptors accounts for the greater part of its effects, only a small part being due to its ability to release norepinephrine. Phenylephrine has no effet on adrenergic receptors of the bronchi or peripheral blood vessels. Phenylephrine has a mild central stimulant effect. Brompheniramine: Brompheniramine is an antihistamine, H1 receptor blocking agent belonging to the alkylamine class of antihistamines. This group of antihistamines are among the most active histamine antagonists and are generally effective in relatively low doses. These drugs are not prone to produce drowsiness and are among the most suitable agents for daytime use; but again, asignificant proportion of patients do experience this effect. INDICATIONS AND USAGE Entre-B is indicated for the symptomatic relief of coryza, nasal congestion associated with the common cold, sinusitis, allergic rhinitis, and other upper respiratory tract conditions. Appropriate therapy should be provided for the primary disease. CONTRAINDICATIONS Entre-B is contraindicated in patients sensitive to any of the ingredients or related compounds. Antihistamines are contraindicated for use in the treatment of lower respiratory tract symptoms, including asthma. Phenylephrine is contraindicated in patients with hypertension or with peripheral vascular insufficiency (ischemia may result with risk of gangrene or thrombosis of compromised vascular beds.) Entre-B should not be used in patients receiving a monoamine oxidase inhibitor (MAOI) (see PRECAUTIONS: DRUG INTERACTIONS) WARNINGS This product contains an antihistamine that may cause drowsiness and may have additive central nervous system (CNS) effects with alcohol or other CNS depressants (e.g., hypnotics, sedatives, tranquilizers). Antihistamines should be used with caution in patients with stenosing peptic ulcer, pyloroduodenal obstruction, and urinary bladder obstruction due to symptomatic prostatic hypertrophy and narrowing of the bladder neck. PRECAUTIONS GENERAL: Antihistamines are more likely to cause dizziness, sedation, and hypotension in elderly patients, and therefore should be used with caution. Antihistamines may cause excitation, particularly in pediatric patients, but their combination with sympathomimetics may cause either mild stimulation or mild sedation. Use with caution in patients with hypertension, cardiovascular disease, hyperthyroidism, diabetes, or narrow angle glaucoma. INFORMATION FOR PATIENTS Caution patients against drinking alcoholic beverages or engaging in potentially hazardous activities requiring alertness, such as driving a car or operating machinery, while using this product. Patients should be warned not to use this product if they are now taking a prescription monoamine oxidase (MAO) inhibitor (certain drugs for depression, psychiatric or emotional conditions, or Parkinson s disease), or for 2 weeks after stopping the MAO inhibitor drug. If patients are uncertain whether the prescription drug contains an MAO inhibitor,they should be instructed to consult a health professional before taking this product. DRUG INTERACTIONS MAO inhibitors may prolong and intensify the anticholinergic effects of antihistamines and the overall effects of sympathomimetic agents. Patients may develop hyperpyrexia, hypotension, nausea, myoclonic leg jerks, and coma following co-administration of MAO. Thus, concomitant administration of Entre-B and MAO inhibitors should be avoided (see CONTRAINDICATIONS). CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY No long-term animal studies have been performed with Entre-B. PREGNANCY Teratogenic Effects Pregnancy Category C: Animal reproduction studies have not been conducted with Entre-B Suspension. It is also not known whether Entre-B can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Entre-B should be given to a pregnant woman only if clearly needed. LABOR AND DELIVERY: Administration of Phenylephrine to patients in late pregnancy or labor may cause fetal anoxia or bradycardia by increasing contractility of the uterus and decreasing uterine bloodflow. NURSING MOTHERS: Because of the higher risk of intolerance of antihistamines in small infants generally, and in newborns and prematures in particular, Entre-B should not be administered to a nursing mother. ADVERSE REACTIONS The most common effects associated with antihistamines have been drowsiness, sedation, dryness of mucous membranes, and gastrointestinal effects. Serious side effects with oral antihistamines and sympathomimetics, have been rare. Other adverse reactions may include: Dermatologic urticaria, drug rash, photosensitivity, pruritus. Cardiovascular hypotension, hypertension, cardiac arrhythmias, palpitations. Central Nervous System (CNS) disturbed coordination, tremor, irritability, insomnia, visual disturbances, weakness, nervousness, convulsion, headache, euphoria and dysphoria. Genitourinary urinary frequency, difficult urination. Gastrointestinal epigastric discomfort, anorexia, nausea, vomiting, diarrhea, constipation. Respiratory tightness of chest and wheezing, shortness of breath. Hematologic hemolytic anemia, thrombocytopenia, agranulocytosis. OVERDOSAGE SIGNS AND SYMPTOMS May vary from CNS depression to stimulation (restlessness to convulsions). Antihistamine overdosage in young children may lead to convulsions and death. Atropine-like signs and symptoms may be prominent. TREATMENT: Induce vomiting if it has not occurred spontaneously. Precautions must be taken against aspiration especially in infants, children and comatose patients. If gastric lavage is indicated, isotonic or half-isotonic saline solution is preferred. Stimulants should not be used. If hypotension is a problem, vasopressor agents may be considered. DOSAGE AND ADMINISTRATION Entre-B: Administer the recommended dose every 12 hours. Adults and Children over 12 years of age 5 to 10mL (1 to 2 teaspoonfuls); Children 6 to 12 years of age 5 mL (1 teaspoonful); Children under 6 years of age consult a physician. HOW SUPPLIED Entre-B Suspension is available as a bubble gum flavored suspension in 4 fl. oz. bottles (NDC 42192-513-04). STORAGE Store at controlled room temperature, 20 - 25 C (68 - 77 F). Dispense in a tight, light-resistant container (USP/NF) with a child-resistant closure. All prescription substitutions and/or recommendations using this product shall be made subject to state and federal statutes as applicable. Please note: this is not an Orange Book product and has not been subjected to FDA therapeutic equivalency or other equivalency testing. Each person recommending a prescription substitution using this product shall make such recommendations based on each such person s professional opinion and knowledge, upon evaluating the active ingredients, excipients, inactive ingredients and chemical information provided herein. MANUFACTURED FOR Acella Pharmaceuticals, LLC Alpharetta, GA 30009 1-800-541-4802 Rev. 0210 Utilizing NeuvosynTM Technology Entre-B Suspension Antihistimine Decongestant Bubblegum Flavor Each 5 mL (teaspoonful) contains: Brompheniramine Maleate.......6 mg Phenylephrine HCl...................10 mg Rx Only Shake Well 4fl oz (118 mL) Acella Pharmaceuticals, LLC DOSAGE AND ADMINISTRATION: Adults and children over 12 years of age: 1 - 2 teaspoonfuls every 12 hours. Children 6 to under 12 years of age: 1 teaspoonful every 12 hours. Children under 6 years of age: Consult a physician. Dispense in a well closed, light-resistant container. Store at controlled room temperature, 20 - 25 C (68 - 77 F) [See USP]. Shake well before use. WARNING: KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY. MANUFACTURED FOR: Acella Pharmaceuticals, LLC 9005 Westside Parkway Alpharetta, GA 30009 Utilizing Neuvosyn Technology Rev. 0210v3 Entre-B brompheniramine maleate, phenylephrine hcl suspension Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:42192-513 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMPHENIRAMINE MALEATE (BROMPHENIRAMINE) BROMPHENIRAMINE MALEATE 6 mg in 5 mL PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE 10 mg in 5 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL GLYCERIN XANTHAN GUM SACCHARIN SODIUM SODIUM CITRATE TANNIC ACID MAGNESIUM ALUMINUM SILICATE BENZOIC ACID METHYLPARABEN PROPYLPARABEN WATER Product Characteristics Color Score Shape Size Flavor BUBBLE GUM (BUBBLEGUM FLAVOR) Imprint Code Contains Packaging # Item Code Package Description 1 NDC:42192-513-04 118 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/11/2010 Labeler - ACELLA PHARMACEUTICALS (825380939) Revised: 12/2010 ACELLA PHARMACEUTICALS Next Interactions Print this page Add to My Med List More about Entre-B (brompheniramine / phenylephrine) Side Effects During Pregnancy Dosage Information Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: upper respiratory combinations Consumer resources Professional resources Other brands: V-HIST Related treatment guides Allergic Rhinitis Nasal Congestion Rhinitis} FEATURED: CAR-T Cell Therapy Overview Mechanism of Action KTE-C19 Studies KTE-C19 Cancer Targets Adverse Events Manufacturing Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug WADA Class Anti-Doping Classification Drug Class Upper respiratory combinations Related Drugs upper respiratory combinations Promethazine DM , Cheratussin AC , Mucinex DM Allergic Rhinitis prednisone , Zyrtec , promethazine , fluticasone nasal , loratadine , cetirizine , Flonase , triamcinolone , More... 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