NDC 17856-0141 Childrens Silapap

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-0141
Proprietary Name:
Childrens Silapap
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Start Marketing Date: [9]
01-15-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - CHERRY FLAVOR)

Product Packages

NDC Code 17856-0141-1

Package Description: 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 20.31 mL in 1 CUP, UNIT-DOSE

NDC Code 17856-0141-2

Package Description: 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 31.25 mL in 1 CUP, UNIT-DOSE

NDC Code 17856-0141-3

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

NDC Code 17856-0141-4

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

NDC Code 17856-0141-5

Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 5 mL in 1 CUP, UNIT-DOSE

NDC Code 17856-0141-6

Package Description: 48 SYRINGE in 1 BOX, UNIT-DOSE / 5 mL in 1 SYRINGE

NDC Code 17856-0141-7

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

NDC Code 17856-0141-8

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

Product Details

What is NDC 17856-0141?

The NDC code 17856-0141 is assigned by the FDA to the product Childrens Silapap which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 17856-0141-1 50 cup, unit-dose in 1 box, unit-dose / 20.31 ml in 1 cup, unit-dose, 17856-0141-2 50 cup, unit-dose in 1 box, unit-dose / 31.25 ml in 1 cup, unit-dose, 17856-0141-3 50 cup, unit-dose in 1 box, unit-dose / 15.6 ml in 1 cup, unit-dose, 17856-0141-4 120 syringe in 1 box, unit-dose / 2.5 ml in 1 syringe, 17856-0141-5 72 cup, unit-dose in 1 box, unit-dose / 5 ml in 1 cup, unit-dose, 17856-0141-6 48 syringe in 1 box, unit-dose / 5 ml in 1 syringe, 17856-0141-7 120 syringe in 1 box, unit-dose / 1.25 ml in 1 syringe, 17856-0141-8 120 syringe in 1 box, unit-dose / 2.5 ml in 1 syringe. 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 Childrens Silapap?

Do not take more than directed (see overdose warning). if needed, repeat dose every 4 hours or as directed by a doctor do not give more than 5 doses in 24 hours children under 2 yrs (under 24 lbs) ask a doctor children 2-3 years (24-35 lbs) 1 teaspoonful (TSP)(5 mL) children 4-5 years (36-47 lbs) 1 1/2 teaspoonfuls (TSP)(7.5 mL) children 6-8 years (48-59 lbs) 2 teaspoonfuls (TSP)(10 mL) children 9-10 years (60-71 lbs) 2 1/2 teaspoonfuls (TSP)(12.5 mL) children 11 years (72-95 lbs) 3 teaspoonfuls (TSP)(15 mL) adults & children 12 years & older 4 teaspoonfuls (TSP)(20 mL)Other information Store at room temperature 20°-25°C (68°-77°F)

Which are Childrens Silapap UNII Codes?

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

Which are Childrens Silapap 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 Childrens Silapap?

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".