1. Home
  2. Labeler Index
  3. Atlantic Biologicals Corp.
  4. NDC Product Code: 17856-0218 Good Neighbor Pharmacy Childrens Pain And Fever

NDC 17856-0218 Good Neighbor Pharmacy Childrens Pain And Fever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 17856-0218?
  5. Good Neighbor Pharmacy Childrens Pain And Fever Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-0218
Proprietary Name:
Good Neighbor Pharmacy Childrens Pain And Fever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Product Label ID:
78f1a2bf-9c12-45b8-93a9-27307d758745
Start Marketing Date: [9]
06-24-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - VISCOUS)
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 17856-0218-1

Package Description: 120 SYRINGE in 1 BOX, UNIT-DOSE / 2.5 mL in 1 SYRINGE

NDC Code 17856-0218-2

Package Description: 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 15.6 mL in 1 CUP, UNIT-DOSE

NDC Code 17856-0218-3

Package Description: 120 SYRINGE in 1 BOX, UNIT-DOSE / 1.25 mL in 1 SYRINGE

NDC Code 17856-0218-4

Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 3.75 mL in 1 CUP, UNIT-DOSE

Product Details

What is NDC 17856-0218?

The NDC code 17856-0218 is assigned by the FDA to the product Good Neighbor Pharmacy Childrens Pain And Fever which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 17856-0218-1 120 syringe in 1 box, unit-dose / 2.5 ml in 1 syringe, 17856-0218-2 50 cup, unit-dose in 1 box, unit-dose / 15.6 ml in 1 cup, unit-dose, 17856-0218-3 120 syringe in 1 box, unit-dose / 1.25 ml in 1 syringe, 17856-0218-4 72 cup, unit-dose in 1 box, unit-dose / 3.75 ml in 1 cup, unit-dose. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Good Neighbor Pharmacy Childrens Pain And Fever?

•this product does not contain directions or complete warnings for adult use•do not give more than directed (see overdose warning)•shake well before using•mL = milliliter•find right dose on chart below. If possible, use weight to dose; otherwise, use age.•remove the child protective cap and squeeze your child’s dose into the dosing cup•repeat dose every 4 hours while symptoms last•do not give more than 5 times in 24 hoursWeight (lb)Age (yr)Dose (mL)*under 24under 2 yearsask a doctor24-352-3 years5 mL36-474-5 years7.5 mL48-596-8 years10 mL60-719-10 years12.5 mL72-9511 years15 mL*or as directed by a doctorAttention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.

Which are Good Neighbor Pharmacy Childrens Pain And Fever UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Good Neighbor Pharmacy Childrens Pain And Fever Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Good Neighbor Pharmacy Childrens Pain And Fever?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Acetaminophen


Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
[Learn More]


Pain Relievers


Pain relievers are medicines that reduce or relieve headaches, sore muscles, arthritis, or other aches and pains. There are many different pain medicines, and each one has advantages and risks. Some types of pain respond better to certain medicines than others. Each person may also have a slightly different response to a pain reliever.

Over-the-counter (OTC) medicines are good for many types of pain. There are two main types of OTC pain medicines: acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs (NSAIDs). Aspirin, naproxen (Aleve), and ibuprofen (Advil, Motrin) are examples of OTC NSAIDs.

If OTC medicines don't relieve your pain, your doctor may prescribe something stronger. Many NSAIDs are also available at higher prescription doses. The most powerful pain relievers are opioids. They are very effective, but they can sometimes have serious side effects. There is also a risk of addiction. Because of the risks, you must use them only under a doctor's supervision.

There are many things you can do to help ease pain. Pain relievers are just one part of a pain treatment plan.


[Learn More]


* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".