COUGH RELIEF- dextromethorphan hbr liquid

Cough Relief by

Drug Labeling and Warnings

Cough Relief by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each 5 mL, 1 teaspoon)

Dextromethorphan HBr, USP 15 mg

Purpose

Cough suppressant

Uses

temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants.

Warnings

Do not use

• if you are on a sodium-restricted diet 
• if you are now 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

• cough that occurs with too much phlegm (mucus)
• persistent or chronic cough such as occurs with smoking, asthma or emphysema

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or is accompanied by fever, rash or headache that lasts. These could be signs of a serious condition.

When using this product

• do not use more than directed

If pregnant or breast-feeding,

ask a health professional before use.

Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

• take recommended dosage or as directed by a doctor
• tsp = teaspoon, mL = milliliter

• age: dose
• adults and children 12 years and over: 2 teaspoonfuls every 6-8 hours, not to exceed 4 doses in 24 hours
• children 6 to under 12 years: 1 teaspoonful every 6-8 hours, not to exceed 4 doses in 24 hours
• children 4 to under 6 years: do not use unless directed by a doctor
• children under 4 years: do not use

Other information

• each teaspoon contains: sodium 6 mg
• store at room temperature

Inactive ingredients

citric acid, edetate disodium, flavor, glycerin, high fructose corn syrup, hydroxyethyl cellulose, polyethylene glycol 3350, propylene glycol, purified water, sodium benzoate, sucralose, sucrose, xanthan gum, yellow 6

Questions or comments?

1-866-534-4631

Principal Display Panel

SEE NEW DOSING INFORMATION 

COUGH RELIEF

Cough Suppressant

Dextromehtorphan HBr

Orange Flavor

Alcohol Free

FL OZ (mL)

Contains no fever reducer or pain reliever

This product is not manufactured or distributed by Reckitt Benckiser, distributor of Delsym® Cough Suppressant.

Distributed by: Chain Drug Consortium, LLC.,

3301 NW Boca Raton Blvd., Suite 101

Boca Raton, FL 33431

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL ON THE BOTTLE IS BROKEN OR MISSING.

Package Label

Premier Value Cough Relief Liquid, Orange flavor

INGREDIENTS AND APPEARANCE

COUGH RELIEF 
dextromethorphan hbr liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-156
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)
XANTHAN GUM (UNII: TTV12P4NEE)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Characteristics
Color		Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-156-04	1 in 1 BOX	03/30/2011	12/31/2020
1		118 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 FINAL	part341	03/30/2011	12/31/2020

Labeler - Chain Drug Consortium, LLC (101668460)