NDC 42961-042 Zee Pain Aid

Acetaminophen Salicylamide Aspirin

NDC Product Code 42961-042

NDC CODE: 42961-042

Proprietary Name: Zee Pain Aid 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 Salicylamide Aspirin 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.

Product Characteristics

Color(s):
ORANGE (C48331 - LIGHT ORANGE)
Shape: ROUND (C48348)
Size(s):
11 MM
Imprint(s):
PA;ZEE
Score: 1

NDC Code Structure

  • 42961 - Cintas Corporation

NDC 42961-042-04

Package Description: 500 CARTON in 1 CARTON > 50 CARTON in 1 CARTON (42961-042-03) > 125 PACKET in 1 CARTON (42961-042-02) > 2 TABLET in 1 PACKET (42961-042-01)

NDC Product Information

Zee Pain Aid with NDC 42961-042 is a a human over the counter drug product labeled by Cintas Corporation. The generic name of Zee Pain Aid is acetaminophen salicylamide aspirin. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Cintas Corporation

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Zee Pain Aid 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 110 mg/1
  • ASPIRIN 162 mg/1
  • SALICYLAMIDE 152 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.

  • STARCH, CORN (UNII: O8232NY3SJ)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)

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: Cintas Corporation
Labeler Code: 42961
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: 01-05-2021 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Zee Pain Aid Product Label Images

Zee Pain Aid 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

Otc - Active Ingredient

Active Ingredient/TabletAcetaminophen 110mg, Aspirin 162 mg-Salicylamide 152 mg,Pain Reviever Aid, Caffeine 32.5 mg-Pain Reliever Aid

Otc - Purpose

Purpose-Pain Reliever/Fever Reducer

Indications & Usage

Temporarily relieves pain dut to: headache, muscular aches, cold, flu.  Temporarily reduces fever

Dosage & Administration

Adults: Take 2 caplets every 6 hours, not to exceed 8 caplets in 24 hoursChildren under 12 years, ask a doctor

Warnings

Liver Warning: This product contains acetaminophen. Severe liver damage     may occur if you take:•    more than 8 tablets in 24 hours •    with other drugs containing acetaminophen (prescription or nonprescription).  Ask a doctor or pharmacist before using with other drugs if you are not sure.  •    3 or more alcoholic drinks every day while using this product______________________________________________________________ Do not use: •    with any other product containing acetaminophen this will provide more  than the recommended dose (overdose) of acetaminophen and could  cause serious health concerns.  •    for more than 10 days for pain unless directed by a doctor •    for more than 3 days for fever unless directed by a doctor •    When using this product do not exceed recommended dose. _______________________________________________________________Stop use and ask a doctor if: •    symptoms do not improve•    pain or fever persists or gets worse •    new symptoms occur•    redness or swelling is present

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding baby, ask a health professional  before use

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. In case of 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.

Inactive Ingredient

Inactive Ingredients: corn starch, microcrystalline cellulose,  povidone,  croscarmellose sodium, FDC Yellow 6, magnesium stearate, and stearic acid

* Please review the disclaimer below.