Label: OTIS CLAPP VALIHIST- acetaminophen,chlorpheniramine maleate, phenylephrine hydrochloride tablet, film coated
MEDIQUE MEDICIDIN D- acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, film coated
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NDC Code(s):
47682-120-13,
47682-120-33,
47682-120-47,
47682-120-64, view more47682-120-99, 47682-543-03, 47682-543-99
- Packager: Unifirst First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
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INDICATIONS & USAGE
Uses
Temporarily relieves
- minor aches and pains
- headache
- nasal congestion
- sinus congestion and pressure
- runny nose
- sneezing
Temporarily
- reduces fever
- relieves runny nose and reduces sneezing, itching of the nose and throat and itchy, watery eyes due to hay fever
- helps clear nasal and/or sinus passages
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WARNINGS
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg of acetaminophen 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.
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DO NOT USE
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
- if you ever had an allergic reaction to this product or any of its 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 DOCTOR
- ASK DOCTOR/PHARMACIST
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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Principal Display Panel - 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
This Package is for Households without Young Children.
Acetaminophen 325 mg,
Chlorpheniramine Maleate 2mg
Phenylephrine HCl 5 mg
Tear Out Along Perforation To Dispense
PROFESSIONAL HEALTHCARE
300 TABLETS (150 PACKETS OF 2)
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Principal Display Panel - Medique Medicidin D Label
Medique®
Medicidin-D
Cold and Allergy Relief
This Package is for Households without Young Children.
Pull to Open
Pain Reliever/ Fever Reducer ● Acetaminophen 325mg
Antihistamine ● Chlorpheniramine Maleate 2mg
Nasal Decongestant ● Phenylephrine HCl 5mg
100Tablets
(50 x 2)
Tamper Evident Unit Dose Packets
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INGREDIENTS AND APPEARANCE
OTIS CLAPP VALIHIST
acetaminophen,chlorpheniramine maleate, phenylephrine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-543 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 2 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) CROSPOVIDONE (UNII: 68401960MK) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 11mm Flavor Imprint Code AZ;275 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-543-03 150 in 1 BOX 12/30/2008 1 NDC:47682-543-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-543-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 12/30/2008 MEDIQUE MEDICIDIN D
acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-120 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 2 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) CROSPOVIDONE (UNII: 68401960MK) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 11mm Flavor Imprint Code AZ;275 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-120-64 12 in 1 BOX 12/30/2008 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-120-33 50 in 1 BOX 12/30/2008 2 2 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:47682-120-47 100 in 1 BOX 12/30/2008 3 2 in 1 PACKET; Type 0: Not a Combination Product 4 NDC:47682-120-13 250 in 1 BOX 12/30/2008 4 NDC:47682-120-99 2 in 1 PACKET; Type 0: Not a Combination Product 5 NDC:47682-120-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 12/30/2008 Labeler - Unifirst First Aid Corporation (832947092)