NDC 47682-903 Medi First Plus Non-aspirin
Acetaminophen
NDC Product 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 InformationThe 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
- 47682 - Unifirst First Aid Corporation
- 47682-903 - Medi First Plus Non-aspirin
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.
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’.
* Please review the disclaimer below.
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)
- Purpose
- Uses
- Other
- Allergy Alert:
- Do Not Use
- Ask A Doctor Before Use If You Have
- Ask A Doctor Or Pharmacist Before Use If
- Stop Using And Ask A Doctor If
- If Pregnant Or Breast-Feeding,
- Keep Out Of Reach Of Children.
- Directions
- Adults And Children: (12 Years And Older)
- Children Under 12 Years:
- Other Information
- Inactive Ingredients
- 145R Medique Apap 325 Mg Label
- Medi-First Non-Aspirin 325 Mg Label
- 145R Mfp Non-Aspirin 325 Mg Label
- Dover Aminofen Label
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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