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  4. NDC Product Code: 59999-001 Childrens Acetaminophen

NDC 59999-001 Childrens Acetaminophen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59999-001?
  5. Childrens Acetaminophen Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59999-001
Proprietary Name:
Childrens Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
R3 Pharmaceuticals, Llc
Labeler Code:
59999
Product Label ID:
de53e048-a13d-4f9b-8e5c-b5449ff47078
Start Marketing Date: [9]
09-23-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 59999-001?

The NDC code 59999-001 is assigned by the FDA to the product Childrens Acetaminophen which is product labeled by R3 Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59999-001-04 1 bottle, plastic in 1 carton / 118 ml in 1 bottle, plastic. 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 Acetaminophen?

Do not give more than directed (see Liver and overdose warning)shake well before usethis product does not contain directions or complete warnings for adult useuse only with enclosed dosing cuprepeat dose every 4 hours if neededdo not give more than 5 times in 24 hoursdo not give for more than 5 days unless directed by a doctorfind right dose on chart below. If possible, use weight to dose, otherwise; use age.Weight (lb)Age (yr)Dose (tsp or mL)under 24under 2 yearsask a doctor24-352-3 years1 tsp or 5 mL36-474-5 years1 1/2 tsp or 7.5 mL48-596-8 years2 tsp or 10 mL60-719-10 years2 1/2 tsp or 12.5 mL72-9511 years3 tsp or 15 mL

Which are Childrens Acetaminophen UNII Codes?

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

Which are Childrens 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:

What is the NDC to RxNorm Crosswalk for Childrens Acetaminophen?

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:

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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".