Supres A

Manufacturer
Dextrum Laboratories, Inc
Effective date
2025-10-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:36

Label at a glance#

ProductSupres A
Active ingredientDEXBROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Label structure9 sections

Dosage and administration

Dosage and administration section Do not use more thab 6 doses in any 24-hour period, repeat ever 4 hour, measure with the dosage device provided. Do not use with any other device. Cildren under 6 years of age, consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Dexbrompheniramine Maleate, 1 mg

Dextromethorphan BBr, 10 mg

Phenylephrine HCL, 5 mg

activeactive

Purpose section

OTC - PURPOSE SECTION

Purpose section

Antihistaminie

Cough suppressant

Nasal descpngestant

purposepurpose

Warnings Section:

WARNINGS SECTION

Warnings Section:

Keep out of reach of childrens. In case of accidental overdose, get medical helpor contacta Poison Control Center right away.

warningswarnings

Keep out of reach of childrens

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrens.

In case of accidental overdose, get medical helpor contacta Poison Control Center right away.

Keep outKeep out

Indication and usage section

INDICATIONS & USAGE SECTION

Indication and usage section

Do not use more thab 6 doses in any 24-hour period, repeat ever 4 hour, measure with the dosage device provided.

Do not use with any other device.

Cildren under 6 years of age, consult a doctor

indicationindication

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Citric acid, flavor, glycerin, methylparaben, polysorbate, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

inactiveinactive

Question section

OTC - QUESTIONS SECTION

Question section:

Question or comments call keekdays from 8 am to 4 pm AST at 1.787.767.2072

questionquestion

Dosage and administration section

DOSAGE & ADMINISTRATION SECTION

Dosage and administration section

Do not use more thab 6 doses in any 24-hour period, repeat ever 4 hour, measure with the dosage device provided.

Do not use with any other device.

Cildren under 6 years of age, consult a doctor

dosagedosage

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

NDC 52083-057-01

Supress A

Antistamine

cough Suppressant

Nasal descongestant

Pedriatic Drops

Sugar, Dye and alcohol free

Pseudoephedrine and PPA free

30ml (1FL OZ)

Kramer Novis

principal panelprincipal panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
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43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
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d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65852-01465852-014-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
407f39f2-4a31-edbd-e063-6294a90a3a34402e779e-def2-131e-e063-6294a90a7efe2025-10-06WarningsExact identifier
spl set id: 402e779e-def2-131e-e063-6294a90a7efe

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.