Label: MEDI-FIRST NON-ASPIRIN- acetaminophen tablet, coated
- NDC Code(s): 71205-306-04
- Packager: Proficient Rx LP
- This is a repackaged label.
- Source NDC Code(s): 47682-803
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
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- Drug Facts
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
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- more than 12 tablets in 24 hours, which is the maximum daily amount
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- with other drugs containing acetaminophen
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- 3 or more alcoholic drinks every day while using this product
Allergy alert:
Acetaminophen may cause severe skin reactions. Symptoms may include:
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- skin reddening
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- blisters
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- rash
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
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- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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- for more than 10 days for pain unless directed by a doctor
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- for more than 3 days for fever unless directed by a doctor
- Directions
- Inactive ingredients
- Questions or comments?
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Medi-First Non-Aspirin 325 mg Label
4 Tablets
71205-306-04
Medi-First ®
Non-Aspirin
Aches, Fever ● Acetaminophen 500mg
Dolores, Fiebre ● Acetaminofeno 500mg
Aspirin-Free Pain Relief
Pull to Open
Tire Para Abrir
Compare active ingredients to:
Compare el ingrediente activo con:
Extra Strength Tylenol®
Registered Trademark of McNeil Consumer Products
Marca Registrada de McNeil Consumer Products
Tamper Evident Unit Dose Packets
Empaquetado con Sellado
Evidente en Dosis Unitarias
Relabeled by:
Proficient Rx LP
Thousand Oaks, CA 91320
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INGREDIENTS AND APPEARANCE
MEDI-FIRST NON-ASPIRIN
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71205-306(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 HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (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:71205-306-04 4 in 1 PACKET; Type 0: Not a Combination Product 08/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 12/30/2008 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 RELABEL(71205-306)