MEDI FIRST SINUS PAIN AND PRESSURE- acetaminophen, phenylephrine hydrochloride tablet 
OTIS CLAPP MYGREX- acetaminophen, phenylephrine hydrochloride tablet 
MEDI FIRST PLUS SINUS PAIN AND PRESSURE- acetaminophen, phenylephrine hydrochloride tablet 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Medi-First Sinus Pain and Pressure

Drug Facts

Active ingredients (in each tablet)

Acetaminophen 500mg

Phenylephrine HCl 5mg

Purpose

Pain reliever/fever reducer

Nasal decongestant

Uses

temporarily relieves these common cold/flu symptoms:

temporarily reduces fever

Warnings

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

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

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.
  • 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.
  • for more than 10 days for pain unless directed by a doctor

Ask a doctor before use if you have

  • liver disease
  • thyroid disease
  • diabetes
  • high blood pressure
  • heart disease
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin

When using this product do not exceed recommended dosage.

Stop use and ask a doctor if

  • you get nervous, dizzy, or sleepless
  • pain or nasal congestion gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms appear

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.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick 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 over) Take 2 tablets every 6 hours. Do not take more than 8 tablets in 24 hours.

Children under 12 years: Ask adoctor

Other information

Inactive ingredients corn starch, crospovidone*, FD&C blue #1*, hypromellose*, microcrystalline cellulose, polyethylene glycol*, povidone, pregelatinized starch*, sodium starch glycolate*, stearic acid.

*may contain

Questions or comments? 1-800-634-7680

Medi-First Plus Sinus Pain and Pressure Label

100 Tablets
(50 x 2's)
Medi First ® Plus
Sinus Pain and Pressure
Aches & Fever • Acetaminophen 500 mg

Nasal Decongestant • Phenylephrine HCl 5 mg

Pull to Open

This Package is For Households Without Young Children.

Sinus Pain Releif

Tamper Evident

Unit Dose Packets

Medi-First

Medi-First Sinus Pain and Pressure Label

250 Tablets
(125 x 2)
Medi-First ®
Sinus Pain and Pressure

Alivio al dolor y presion en los

senos nasales

Pull to Open
Tire Para Abrir

Aches & Fever • Acetaminophen 500 mg

Dolores, Fiebre • Acetaminofeno 500 mg

Nasal Decongestant • Phenylephrine HCl 5 mg

Descongestivo nasal • Hidrocloruro de fenilefrina 5 mg

This Package is For Households Without Young Children.

Este Paquete Es Para Hogares Sin Ninos Pequenos.

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Rvidente en Dosis Unitarias

MF Sinus

Otis Clapp Mygrex Label

Otis Clapp
Quality and Integrity Since 1840
MYGREX ™
Pain Reliever-Decongestant
Advanced Relief
For Sinus/Headaches
See Warnings and Directions on Side Panel

This Package is for Households without Young Children.
Acetaminophen 500 mg • Aches & Fever
Phenylephrine HCl 5 mg • Nasal Decongestant
Tear Out Along Perforation To Dispense
PROFESSIONAL HEALTHCARE
300 Tablets (150 PACKETS OF 2)

Otis

MEDI FIRST SINUS PAIN AND PRESSURE 
acetaminophen, phenylephrine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-146
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
STEARIC ACID (UNII: 4ELV7Z65AP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorblue (blue) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorImprint Code FR;33
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-146-3350 in 1 BOX12/30/2008
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-146-48125 in 1 BOX12/30/2008
22 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-146-13250 in 1 BOX12/30/2008
3NDC:47682-146-992 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-146-992 in 1 PACKET; Type 0: Not a Combination Product12/30/2008
5NDC:47682-146-5025 in 1 BOX04/16/2019
52 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34112/30/2008
OTIS CLAPP MYGREX 
acetaminophen, phenylephrine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-148
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorblue (blue) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorImprint Code FR;33
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-148-03150 in 1 BOX12/30/2008
1NDC:47682-148-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-148-992 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 finalpart34112/30/2008
MEDI FIRST PLUS SINUS PAIN AND PRESSURE 
acetaminophen, phenylephrine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-158
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorblue (blue) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorImprint Code FR;33
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-158-3350 in 1 BOX12/30/2008
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-158-48125 in 1 BOX12/30/2008
22 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34112/30/2008
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 3/2022
Document Id: da5abd5c-edeb-a61b-e053-2995a90a39eb
Set id: 8aa33e28-f1d4-42f0-a334-bf85a779fe3f
Version: 15
Effective Time: 20220316
 
Unifirst First Aid Corporation