MEDIQUE DECOREL FORTE PLUS - acetaminophen, dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride tablet, film coated
MEDI-FIRST COLD RELIEF - acetaminophen, dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride tablet, film coated
MEDI-FIRST PLUS COLD RELIEF - acetaminophen, dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride tablet, film coated
Unifirst First Aid Corporation

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425R Decorel Forte Plus UniFirst 47682 Medique, MF/MFP

Drug Facts

Active ingredients (in each tablet)

Acetaminophen 325 mg

Dextromethorphan Hydrobromide 15mg

Guaifenesin 200mg

Phenylephrine Hydrochloride 5mg

Purposes

Pain reliever/ fever reducer

Cough suppressant

Expectorant

Nasal decongestant

Uses

Temporarily relieves these cold symptoms

cough
sore throat
minor aches and pains
headache
nasal congestion
helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Temporarily reduces fever.

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

more than 8 tablets in 24 hours, which is the maximum daily amount for this product
with other drugs containing acetaminophen
3 or more alcoholic drinks every day while using this product

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

Do not use

with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
with any other product containing any of the above active ingredients
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

liver disease
heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostate gland
cough that occurs with too much phlegm (mucus)
chronic cough that lasts as occurs with smoking, asthma, chronic bronchitis or emphysema

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers
taking the blood thinning drug warfarin

When using this product

do not use more than directed
excitability may occur, especially in children
marked drowsiness may occur
alcohol, sedatives and tranquilizers may increase the drowsiness effect
avoid alcoholic drinks
be careful driving a motor vehicle or operating machinery

Stop use and ask a doctor if

new symptoms occur
redness or swelling is present
pain or nasal congestion gets worse or lasts for more than 7 days
fever gets worse or lasts for more than 3 days
you get nervous, dizzy or sleepless
cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Adults and children: (12 years and older)

Take 2 tablets with water every 6- 8 hours as needed. Do not take more than 8 tablets in 24 hours.

Children under 12 years:

Do not give to children under 12 years of age.

Other information

store at room temperature 59°-86°F (15°-30°C)
avoid excessive heat and humidity
tamper evident sealed packets
do not use any opened or torn packets

Inactive ingredients

croscarmellose sodium*, hypromellose*, maltodextrin*, microcrystalline cellulose, polyethylene glycol*, povidone*, sodium starch glycolate*, starch, stearic acid.

*may contain

Questions or comments? 1-800-634-7680

425R Medique Decorel Forte Plus Label

Medique®

Decorel Forte Plus

See new warnings information

Acetaminophen 325mg

Dextromethorphan HBr 15mg

Guaifenesin 200mg

Phenylephrine HCl 5mg

Pull to Open

Easy To Swallow

Film Coated Tablets

100 Tablets

(50 x 2)

Severe Cold and Cough Relief

Tamper Evident Unit Dose Packets

425R MF Cold Relief Label

100 Tablets

(50 x 2)

Medi-First®

Cold Relief Multi-Symptom

Acetaminophen 325mg

Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl

Pull to Open

Easy To Swallow

Film Coated Tablets

See new warnings information

Tamper Evident Unit Dose Packets

425R MFP Cold Relief Label

100 Tablets

(50 x 2's)

Medi-First® Plus

Cold Relief

Multi-Symptom

Acetaminophen 325mg

Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl

Pull to Open

Easy To Swallow

Film Coated Tablets

See new warnings information

Tamper Evident Unit Dose Packets

MEDIQUE DECOREL FORTE PLUS
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	47682-425
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (ACETAMINOPHEN)	ACETAMINOPHEN	325 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg
GUAIFENESIN (GUAIFENESIN)	GUAIFENESIN	200 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE)	PHENYLEPHRINE HYDROCHLORIDE	5 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
POLYETHYLENE GLYCOL
STARCH, CORN
STEARIC ACID

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	12mm
Flavor		Imprint Code	AZ;273
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	47682-425-33	50 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET (47682-425-99)
1	47682-425-99	2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-425-33)
2	47682-425-13	250 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET (47682-425-99)
2	47682-425-99	2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-425-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	12/30/2008

MEDI-FIRST COLD RELIEF
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	47682-822
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (ACETAMINOPHEN)	ACETAMINOPHEN	325 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg
GUAIFENESIN (GUAIFENESIN)	GUAIFENESIN	200 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE)	PHENYLEPHRINE HYDROCHLORIDE	5 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
POLYETHYLENE GLYCOL
STARCH, CORN
STEARIC ACID

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	12mm
Flavor		Imprint Code	AZ;273
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	47682-822-33	50 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET (47682-822-99)
1	47682-822-99	2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-822-33)
2	47682-822-48	125 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET (47682-822-99)
2	47682-822-99	2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-822-48)
3	47682-822-13	250 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET (47682-822-99)
3	47682-822-99	2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-822-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	12/30/2008

MEDI-FIRST PLUS COLD RELIEF
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	47682-922
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (ACETAMINOPHEN)	ACETAMINOPHEN	325 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg
GUAIFENESIN (GUAIFENESIN)	GUAIFENESIN	200 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE)	PHENYLEPHRINE HYDROCHLORIDE	5 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
POLYETHYLENE GLYCOL
STARCH, CORN
STEARIC ACID

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	12mm
Flavor		Imprint Code	AZ;273
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	47682-922-33	50 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET
1		2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-922-33)
2	47682-922-48	125 PACKET In 1 BOX, UNIT-DOSE	contains a PACKET
2		2 TABLET In 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-922-48)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	12/30/2008

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 06/2010Unifirst First Aid Corporation