NDC 47682-903 Medi First Plus Non-aspirin

Acetaminophen

  1. Labeler Index
  2. Unifirst First Aid Corporation
  3. NDC: 47682-903 Medi First Plus Non-aspirin

NDC Product Code 47682-903

NDC CODE: 47682-903

Proprietary Name: Medi First Plus Non-aspirin What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Acetaminophen What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape: ROUND (C48348)
Size(s):
10 MM
Imprint(s):
AZ;234
AZ;234
Score: 1

NDC Code Structure

NDC 47682-903-33

Package Description: 50 PACKET in 1 BOX > 2 TABLET, COATED in 1 PACKET

NDC 47682-903-48

Package Description: 125 PACKET in 1 BOX > 2 TABLET, COATED in 1 PACKET

NDC Product Information

Medi First Plus Non-aspirin with NDC 47682-903 is a a human over the counter drug product labeled by Unifirst First Aid Corporation. The generic name of Medi First Plus Non-aspirin is acetaminophen. The product's dosage form is tablet, coated and is administered via oral form.

Labeler Name: Unifirst First Aid Corporation

Dosage Form: Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Medi First Plus Non-aspirin Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • ACETAMINOPHEN 325 mg/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • 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)
  • 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)
  • 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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Unifirst First Aid Corporation
Labeler Code: 47682
FDA Application Number: part343 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 12-30-2008 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Information for Patients

Acetaminophen

Acetaminophen is pronounced as (a set a mee' noe fen)

Why is acetaminophen medication prescribed?
Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to va...
[Read More]

* Please review the disclaimer below.

Medi First Plus Non-aspirin Product Label Images

Medi First Plus Non-aspirin Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (In Each Tablet)

Acetaminophen 325 mg

Purpose

Pain reliever/fever reducer

Uses

  • For the temporary relief of minor aches and pains associated withheadachecommon coldmuscular achestoothacheminor arthritis painmenstrual crampsFor the reduction of fever.

Other

  • 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 reddeningblistersrashIf 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 doctorfor more than 3 days for fever unless directed by a doctor

Ask A Doctor Before Use If You Have

  • Liver disease

Ask A Doctor Or Pharmacist Before Use If

  • You are taking the blood thinning drug warfarin

Stop Using And Ask A Doctor If

  • Symptoms do not improvenew symptoms occurpain or fever persists or gets worseredness or swelling is present

If Pregnant Or Breast-Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

In case of accidental 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 to 6 hours as needed. 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 59°-86°F (15°-30°C)tamper-evident sealed packetsdo not use any opened or torn packets

Inactive Ingredients

Corn starch, hypromellose, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone*, pregelatinized starch*, sodium starch glycolate*, stearic acid, titanium dioxide** may contain

145R Medique Apap 325 Mg Label

Medique
®APAPNon-Aspirin TabletsPull to OpenPain Reliever/Fever Reducer • Acetaminophen 325 mg150 Tablets(75 x 2)Tamper Evident Unit Dose Packets

Medi-First Non-Aspirin 325 Mg Label

250Tablets(125 x 2)Medi-First
®Non-AspirinAches, Fever ● Acetaminophen 500mgDolores, Fiebre ● Acetaminofeno 500mgAspirin-Free Pain ReliefPull to OpenTire Para AbrirCompare active ingredients to:Compare el ingrediente activo con:Extra Strength Tylenol®Registered Trademark of McNeil Consumer ProductsMarca Registrada de McNeil Consumer ProductsTamper Evident Unit Dose PacketsEmpaquetado con SelladoEvidente en Dosis Unitarias

145R Mfp Non-Aspirin 325 Mg Label

250Tablets(125 x 2's)Medi First
® Plus
Non-AspirinPain Reliever/Fever ReducerAlivia el dolar/Reduce la fiebreAcetaminophen/
Acetaminofeno 325mg
Pull to OpenTire Para AbrirEasy To SwallowFilm Coated TabletsFacil de Tragar Tabletas con Cubierta PelicularCompare active ingredient to:Compare el ingrediente activo con:Extra Strength Tylenol®Registered Trademark of McNeil Consumer ProductsMarca Registrada de McNeil Consumer ProductsTamper Evident Unit Dose PacketsEmpaquetado con SelladoEvidente en Dosis Unitarias

Dover Aminofen Label

Dover AminophenPain Reliever-Fever ReducerNon-Aspirin AnalgesicAcetaminophen 325mgDover PharmaceuticalProducts of the highest quality and effectivenessTamper ResistantSealed PacketsUnit Dose Packs500 Tablets(250 Packets of 2)

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