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NDC 52083-0057-01 SUPRESS A 1; 10; 5 mg/mL; mg/mL; mg/mL Details
SUPRESS A 1; 10; 5 mg/mL; mg/mL; mg/mL
SUPRESS A is a ORAL SYRUP in the HUMAN OTC DRUG category. It is labeled and distributed by Kramer Novis. The primary component is DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Brompheniramine relieves red, irritated, itchy, watery eyes; sneezing; and runny nose caused by allergies, hay fever, and the common cold. Brompheniramine helps control symptoms, but does not treat the cause of the symptoms or speed recovery. Brompheniramine should not be used to cause sleepiness in children. Brompheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Related Packages: 52083-0057-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Brompheniramine
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
Related Packages: 52083-0057-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Dextromethorphan
Phenylephrine is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.
Related Packages: 52083-0057-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Phenylephrine
Product Information
NDC | 52083-0057 |
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Product ID | 52083-057_f3752319-1292-4d33-8d94-37b5a295b265 |
Associated GPIs | 43995803500940 |
GCN Sequence Number | 069948 |
GCN Sequence Number Description | d-methorphan/pe/dexbromphenir DROPS 10-5 MG/ML ORAL |
HIC3 | B3R |
HIC3 Description | NON-OPIOID ANTITUS-1ST GEN.ANTIHISTAMINE-DECONGEST |
GCN | 33223 |
HICL Sequence Number | 025559 |
HICL Sequence Number Description | DEXTROMETHORPHAN HBR/PHENYLEPHRINE HCL/DEXBROMPHENIRAMINE |
Brand/Generic | Brand |
Proprietary Name | SUPRESS A |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Dexbromopheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl |
Product Type | HUMAN OTC DRUG |
Dosage Form | SYRUP |
Route | ORAL |
Active Ingredient Strength | 1; 10; 5 |
Active Ingredient Units | mg/mL; mg/mL; mg/mL |
Substance Name | DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Labeler Name | Kramer Novis |
Pharmaceutical Class | Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 52083-0057-01 (52083005701)
NDC Package Code | 52083-057-01 |
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Billing NDC | 52083005701 |
Package | 30 mL in 1 BOTTLE, PLASTIC (52083-057-01) |
Marketing Start Date | 2012-08-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL f0bec5f5-4d76-471e-9024-557eba848b93 Details
Active ingredients (in each 1 mL)
Uses
- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- sneezing
- itchy nose or throat
- runny nose
- itchy, watery eyes
- nasal congestion
- temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
- temporarily restores freer breathing through nose
Warnings
Do not use in a child who is taking a prescription monoamine oxidase inhibitor (MAOI) (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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- glaucoma
- cough that occurs with too much phlegm (mucus)
- a breathing problem or chronic cough that lasts or occurs with smoking, asthma, chronic bronchitis, or emphysema
- Ask a doctor or pharmacist before use if the child is taking sedatives or tranquilizers
- do not exceed recommended dosage
- excitability may occur, especially in children
- may cause marked drowsiness
- sedative and tranquilizers may increase drowsiness effect
SPL UNCLASSIFIED SECTION
Stop use and ask a doctor if
- nervousness dizziness, or sleeplessness occur
- new symptoms occur
- symptoms do not improve within 7 days or are accompanied by fever
- cough lasts more than 7 days, comes back or is accompanied by fever, rash, or persistent headache
These could be signs of a serious condition.
Keep out of reach of children.
Directions
Other information
Inactive ingredients
SPL UNCLASSIFIED SECTION
INGREDIENTS AND APPEARANCE
SUPRESS A
dexbromopheniramine maleate, dextromethorphan hbr, phenylephrine hcl syrup |
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Labeler - Kramer Novis (090158395) |
Registrant - KRAMER NOVIS (090158395) |