NDC 17856-0985 Childrens Mapap Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0985 - Childrens Mapap Acetaminophen
Product Characteristics
Product Packages
NDC Code 17856-0985-2
Package Description: 2.5 mL in 1 SYRINGE
NDC Code 17856-0985-4
Package Description: 1.25 mL in 1 SYRINGE
NDC Code 17856-0985-5
Package Description: 7.5 mL in 1 SYRINGE
NDC Code 17856-0985-7
Package Description: 5 mL in 1 SYRINGE
NDC Code 17856-0985-8
Package Description: 6.25 mL in 1 SYRINGE
NDC Code 17856-0985-9
Package Description: 2.5 mL in 1 SYRINGE
Product Details
What is NDC 17856-0985?
What are the uses for Childrens Mapap Acetaminophen?
Which are Childrens Mapap Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Childrens Mapap Acetaminophen 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Childrens Mapap Acetaminophen?
- RxCUI: 209397 - Mapap Childrens 160 MG in 5 mL Oral Solution
- RxCUI: 209397 - acetaminophen 32 MG/ML Oral Solution [Mapap]
- RxCUI: 209397 - APAP 32 MG/ML Oral Solution [Mapap]
- RxCUI: 209397 - Mapap 160 mg per 5 mL Oral Solution
- RxCUI: 209397 - Mapap 32 MG/ML Oral Solution
* 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.
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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.
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* Please review the disclaimer below.
[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".