MEDIQUE MEDICIDIN D- acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, coated 
OTIS CLAPP VALIHIST- acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, coated 
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.

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Medique Medicidin D / Otis Clapp Valihist

Drug Facts

Active ingredients (in each tablet)

Acetaminophen 325 mg

Chlorpheniramine Maleate 2 mg

Phenylephrine Hydrochloride 5 mg

Purpose

Pain reliever/fever reducer

Antihistamine

Nasal decongestant

Uses

Temporarily relieves minor aches and pains associated with

  • headache
  • muscular aches
  • minor arthritis pain
  • common cold
  • toothache
  • menstrual cramps

Temporarily relieves nasal congestion due to

  • common cold
  • hay fever or other respiratory allergies

Temporarily

  • reduces fever
  • relieves runny nose and reduces sneezing, itching of the nose and throat and itchy, watery eyes due to hay fever
  • promotes nasal and/or sinus drainage; relieves sinus congestion and pressure

Warnings

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

  • more than 12 tablets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

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

skin reddening

■ blisters

■ rash

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.
  • for more than 10 days for pain unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor
  • with any other drug using 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
  • thyroid disease
  • diabetes
  • high blood pressure
  • heart disease
  • glaucoma
  • chronic bronchitis or emphysema
  • difficulty in urination due to enlargement of the prostate gland

When using this product

  • drowsiness may occur
  • avoid alcoholic beverages
  • alcohol, sedatives and tranquilizers may increase the drowsiness effect
  • use caution when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

Stop use and ask a doctor if

  • symptoms do not improve within 7 days or are accompanied by a fever
  • pain or fever persists or gets worse
  • redness or swelling is present
  • any new symptoms appear

Do not exceed recommended dosage. If nervousness, dizziness or sleeplessness occurs, discontinue use and consult a doctor.

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

  • do not use more than directed

Adults and children: (12 years and older) Take 2 tablets every 4 hours. Do not take more than 12 tablets in 24 hours.

Children under 12 years: Do not give to children under 12 years of age.

Other information

  • store at room temperature 59º-86ºF (15º-30ºC)
  • tamper evident sealed packets
  • do not use any opened or torn packets
  • avoid excessive heat and humidity

Inactive ingredients

corn starch, crospovidone*, hypromellose, maltodextrin*, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch*, sodium starch glycolate*, stearic acid

*may contain.

Questions or comments? 1-800-634-7680

Otis Clapp Valihist Label

Otis Clapp

Quality and Integrity Since 1840

VALIHIST ™

Decongestant-Antihistamine

Pain Reliever-Fever Reducer

Antihistamine-Decongestant

For Allergies, Colds, Runny Nose

See Warnings and Directions on Side Panel

Acetaminophen 325 mg,

Chlorpheniramine Maleate 2mg

Phenylephrine HCl 5 mg

Tear Out Along Perforation To Dispense

PROFESSIONAL HEALTHCARE

New Formula

300 TABLETS (150 PACKETS OF 2) OC Valihist Label 2

Medique Medicidin D Label

Medique®

Medicidin-D

Cold & Alergy

This Package is for Households without Young Children

Pull To Open

Pain Reliever/ Fever Reducer • Acetasminoiphen 325 mg

Antihistamemine • Chlorpheniramine HCl 2 mg

Nasal Decongestant • Phenylephrine HCl 5 mg

100 Tablets

(50 x 2)

Tamper Evident Unit Dose Packets

MDQ MedicidinD

MEDIQUE MEDICIDIN D 
acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-189
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;11
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-189-6412 in 1 BOX03/19/201204/01/2021
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-189-3350 in 1 BOX03/19/201204/01/2021
22 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-189-47100 in 1 BOX03/19/201204/01/2021
32 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-189-13250 in 1 BOX03/19/201204/01/2021
4NDC:47682-189-992 in 1 PACKET; Type 0: Not a Combination Product
5NDC:47682-189-992 in 1 PACKET; Type 0: Not a Combination Product03/19/201204/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/19/201204/01/2021
OTIS CLAPP VALIHIST 
acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-190
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;11
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-190-03150 in 1 BOX03/19/201204/01/2021
1NDC:47682-190-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-190-992 in 1 PACKET; Type 0: Not a Combination Product03/19/201204/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/19/201204/01/2021
Labeler - Unifirst First Aid Corporation (832947092)
Establishment
NameAddressID/FEIBusiness Operations
Prestige Packaging170837962relabel(47682-189, 47682-190) , repack(47682-189, 47682-190)

Revised: 11/2019
 
Unifirst First Aid Corporation