SUPRES A- dexbrompheniramine meleate, dextromethorphan hbr, phenylephrine hcl syrup

Supres A by

Drug Labeling and Warnings

Supres A by is a Otc medication manufactured, distributed, or labeled by Dextrum Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Active ingredient

Dexbrompheniramine Maleate, 1 mg

Dextromethorphan BBr, 10 mg

Phenylephrine HCL, 5 mg

Purpose section

Purpose section

Antihistaminie

Cough suppressant

Nasal descpngestant

Warnings Section:

Warnings Section:

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

Keep out of reach of childrens

Keep out of reach of childrens.

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

Indication and 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

Inactive Ingredients

Inactive Ingredients:

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

Question section

Question section:

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

Dosage and 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

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

INGREDIENTS AND APPEARANCE

SUPRES A 
dexbrompheniramine meleate, dextromethorphan hbr, phenylephrine hcl syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65852-014
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP)	DEXBROMPHENIRAMINE MALEATE	1 mg  in 1 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 1 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SUCRALOSE (UNII: 96K6UQ3ZD4)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CITRIC ACID (UNII: 2968PHW8QP)

Product Characteristics
Color		Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65852-014-01	1 in 1 CARTON	08/01/2012
1		30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	08/01/2012

Labeler - Dextrum Laboratories, Inc (007392322)