NDC 66689-055 Acetaminophen


NDC Product Code 66689-055

NDC Product Information

Acetaminophen with NDC 66689-055 is a a human over the counter drug product labeled by Vistapharm, Inc.. The generic name of Acetaminophen is acetaminophen. The product's dosage form is solution and is administered via oral form.

Labeler Name: Vistapharm, Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

Acetaminophen 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 160 mg/5mL

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.

  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • WATER (UNII: 059QF0KO0R)

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.
  • 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: Vistapharm, Inc.
Labeler Code: 66689
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: 11-22-2019 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: 12-31-2020 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.

Acetaminophen 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 10.15 Ml)

Acetaminophen 325 mg


Pain reliever/fever reducer


■ temporarily relieves minor aches and pains due to:■ headache■ muscle aches■ backache■ minor pain of arthritis■ the common cold■ toothache■ premenstrual and menstrual cramps■ temporarily reduces fever

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

Stop Use And Ask A Doctor If

■ pain gets worse or lasts more than 10 days■ fever gets worse or lasts more than 3 days■ new symptoms occur■ redness or swelling is presentThese could be signs of a serious condition.


■ do not take more than directed (see overdose warning)■ do not take more than 8 doses in any 24-hour period■ dose as follows or as directed by doctor■ take only with dosing cup provided■ adults and children 12 years of age and older: 10.15 mL (325 mg) every 3 - 4 hours■ children under 12 years of age: ask a doctor

Other Information

■ each 10.15 mL contains: sodium 16 mg■ store at 20 -25°C (68 -77°F)■ do not use if foil on cup is missing or torn

Inactive Ingredients

Anhydrous citric acid, FD&C blue no. 1, FD& C red no. 40, flavor, glycerin, methylparaben, polyethylene glycol, propylparaben, purified water, sodium citrate, sodium saccharin

How Supplied

NDC 66689-055-01: 10.15 mL unit-dose cupNDC 66689-055-99: Case contains 100 unit-dose cups of 10.15 mL (NDC 66689-055-01), packaged in 10 trays of 10 unit-dose cups each.Distributed by:VistaPharm Inc.Largo, FL 33771, USAVP251110/2019

* Please review the disclaimer below.