Label: MEDIQUE APAP- acetaminophen tablet, coated
MEDI-FIRST NON-ASPIRIN- acetaminophen tablet, coated
MEDI FIRST PLUS NON-ASPIRIN- acetaminophen tablet, coated
DOVER AMINOPHEN- acetaminophen tablet, coated
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NDC Code(s):
47682-145-13,
47682-145-32,
47682-145-36,
47682-145-48, view more47682-145-64, 47682-145-99, 47682-303-13, 47682-303-99, 47682-803-13, 47682-803-33, 47682-803-48, 47682-803-50, 47682-803-92, 47682-803-99, 47682-903-33, 47682-903-48
- Packager: Unifirst First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated January 10, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg 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.
- if you are allergic to acetaminophen or any of the inactive ingredients in this product
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DOSAGE & ADMINISTRATION
Directions
- do not use more than directed (see overdose warning)
Adults and children: (12 years and over)
- take 2 tablets every 4 to 6 hours while symptoms last.
- do not take more than 10 tablets in 24 hours, unless directed by a doctor
- do not use for more than 10 days unless directed by a doctor
Children under 12 years:
- ask a doctor
- INACTIVE INGREDIENT
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
Medique ®
APAP
Non-Aspirin Tablets
Tabletas sin aspirina
Pain Reliever/Fever Reducer • Acetaminophen 325 mg
Alivia el Dolor/Reduce la Fiebre • Acetaminofeno 325 mg
This Package is For Households Without young Children
Este Paquete es Para Hogares sin Ninos Pequenos
Pull to Open
Tira Para Abrir
500 Tablets
(250 x 2)
Tamper Evident Unit Dose Packets
Empaquetado con Sellado Evidente en Dosis Unitarias
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PRINCIPAL DISPLAY PANEL
Medi-First ®
Non-Aspirin
Aches, Fever ● Acetaminophen 325 mg
Dolores, Fiebre Acetaminofeno 325 mg
Compare active ingredient to:
Tylenol®
Compare el ingredient active con:
Tylenol®
Registerd Trademark of McNeil Consumer products
Marca Registrada de McNeil Consumer Products
Pull to Open
Tira Para Abrir
Pain Reliever/Fever Reducer
Alivia el Dolor/Reduce la Fiebre
This Package is For Households Without Young Children
Este Paquete es Para Hogares sin Ninos Pequenos
Tamper Evident Unit Dose Packets
Empaquetado con Sellado Evidente en Dosis Unitarias
500
Tablets
(250 x 2)
- MFP Non-Aspirin 325 mg Label
-
PRINCIPAL DISPLAY PANEL
Dover Aminofen
Acetaminophen 325 MG
Pain Reliever-Fever Reducer
This Package is for Households withoutn Young Children.
Dover Pharmaceutical
Products of the highest quality and effectiveness
Tamper Evident
Sealed Packets
Unit Dose Packs
500 Tablets
(250 Packets of 2)
All Dover Pharmaceutical formulas conform to federal regulations
Antihistamine free
No danger of drowsiness
Sugar Free
for safer use by diabetics
Salt free
Minimizes high blood pressure
Caffeine Free
Avoides over stimulation
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INGREDIENTS AND APPEARANCE
MEDIQUE APAP
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-145 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code AZ;234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-145-32 6 in 1 BOX 12/30/2008 08/01/2018 1 NDC:47682-145-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-145-64 12 in 1 BOX 12/30/2008 2 NDC:47682-145-99 2 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:47682-145-36 75 in 1 BOX 12/30/2008 3 NDC:47682-145-99 2 in 1 PACKET; Type 0: Not a Combination Product 4 NDC:47682-145-48 125 in 1 BOX 12/30/2008 4 NDC:47682-145-99 2 in 1 PACKET; Type 0: Not a Combination Product 5 NDC:47682-145-13 250 in 1 BOX 12/30/2008 5 NDC:47682-145-99 2 in 1 PACKET; Type 0: Not a Combination Product 6 NDC:47682-145-99 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 not final part343 12/30/2008 MEDI-FIRST NON-ASPIRIN
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-803 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code AZ;234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-803-33 50 in 1 BOX 12/30/2008 1 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-803-48 125 in 1 BOX 12/30/2008 2 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:47682-803-13 250 in 1 BOX 12/30/2008 3 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product 4 NDC:47682-803-92 750 in 1 BOX 12/30/2008 12/01/2022 4 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product 5 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008 6 NDC:47682-803-50 25 in 1 BOX 06/03/2019 6 NDC:47682-803-99 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 12/30/2008 MEDI FIRST PLUS NON-ASPIRIN
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-903 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code AZ;234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-903-33 50 in 1 BOX 12/30/2008 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-903-48 125 in 1 BOX 12/30/2008 2 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 12/30/2008 DOVER AMINOPHEN
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-303 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) HYPROMELLOSES (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code AZ;234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-303-13 250 in 1 BOX 12/30/2008 1 NDC:47682-303-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-303-99 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 not final part343 12/30/2008 Labeler - Unifirst First Aid Corporation (832947092)