MEDIQUE MEDI-PHENYL- phenylephrine hydrochloride tablet, film coated 
DOVER SUDANYL PE- phenylephrine hydrochloride tablet, film coated 
Unifirst First Aid Corporation

----------

Medique and Dover Phenylephrine HCl 5mg

Drug Facts

Active ingredient (in each tablet)

Phenylephrine HCl 5mg

Purpose

Nasal decongestant

Uses

Temporarily relieves

■ nasal congestion due to the common cold, hay fever or other upper respiratory allergies

■ sinus congestion and pressure

Warnings

Do not use

When using this product

do not exceed recommended dosage

Ask a doctor before use if you have

Stop use and ask a doctor if

■ you get nervous, dizzy, or sleepless

■ symptoms do not improve within 7 days or are accompanied by fever

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 (1-800-222-1222).

Directions

Adults and children: (12 years and older)

Take 2 tablets every 4-6 hours. Do not take more than 12 tablets in 24 hours.

Children under 12 years:

Ask a doctor

Other information

Inactive ingredients

croscarmellose sodium, FD&C red #40, FD&C yellow #6, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, propylene glycol, silicon dioxide, titanium dioxide

Questions or comments? 1-800-634-7680

205R Medique Medi-Phenyl Label

Medique®
Medi-Phenyl
Pseudoephedrine Free

Sin seudoefedrina

Nasal Decongestant • Phenylephrine HCl 5mg

Decongestivo Nasal • Hidrocloruro de fenilefrina 5 mg

Pull to Open

Tire Para Abrir

500 Tablets
(250 x 2)
Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

Medique

Dover Sudanyl Label

Dover Sudanyl PE
Nasal and Nasal Decongestant
Non-Drowsy, Sugar Free
Phenylephrine HCl 5mg
Dover Pharmaceutical
Products of the highest quality and effectiveness
Tamper Resistant
Sealed Packets
Unit Dose Packs
500 Tablets
(250 Packets of 2)

Dover

MEDIQUE MEDI-PHENYL 
phenylephrine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-161
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Colorred (red) Scoreno score
ShapeROUND (ROUND) Size7mm
FlavorImprint Code 271
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-161-33100 in 1 BOX12/30/200805/31/2027
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-161-13500 in 1 BOX12/30/200808/31/2027
2NDC:47682-161-992 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-161-992 in 1 PACKET; Type 0: Not a Combination Product12/30/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/30/2008
DOVER SUDANYL PE 
phenylephrine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-162
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Colorred (red) Scoreno score
ShapeROUND (ROUND) Size7mm
FlavorImprint Code 271
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-162-13500 in 1 BOX12/30/200808/31/2027
1NDC:47682-162-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-162-992 in 1 PACKET; Type 0: Not a Combination Product12/30/200808/31/2027
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/30/200808/31/2027
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 9/2025
Document Id: 3e4c212c-9fa3-9a39-e063-6294a90a7f2e
Set id: d7d62ac1-1333-4366-884b-26537766ce38
Version: 13
Effective Time: 20250908
 
Unifirst First Aid Corporation