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  4. NDC Product Code: 76281-302 Childrens Pain And Fever

NDC 76281-302 Childrens Pain And Fever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76281-302?
  4. Childrens Pain And Fever Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
76281-302
Proprietary Name:
Childrens Pain And Fever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aptapharma Inc.
Labeler Code:
76281
Product Label ID:
eda2a4bd-9bb2-46a7-961d-e3aa1519f67b
Start Marketing Date: [9]
08-21-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76281-302-24

Package Description: 118 mL in 1 BOTTLE

Product Details

What is NDC 76281-302?

The NDC code 76281-302 is assigned by the FDA to the product Childrens Pain And Fever which is product labeled by Aptapharma Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76281-302-24 118 ml in 1 bottle . 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 Pain And Fever?

This product does not contain directions or complete warnings for adult useshake well before usingmL = milliliter;   tsp = teaspoonfulfind the right dose on the chart below. If possible, use weight to dose, otherwise, use age.if needed, repeat dose every 4 hours while symptoms lastdo not give more than 5 times in 24 hoursdo not give for more than 5 days unless directed by a doctor.Weight (lb)                                      Age (yr)                                        Dose (mL or  tsp)*under 24                                     under 2 years                                      ask a doctor24-35                                              2 - 3 years                                      5 mL (1 tsp)36-47                                              4 - 5 years                                      7.5 mL (1 1/2 tsp048-59                                              6 - 8 years                                      10 mL (2 tsp)60-71                                             9 - 10 years                                     12.5. mL (2 1/2 TSP)72-95                                                  11 years                                     15 mL (3 tsp)*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 Childrens Pain And Fever UNII Codes?

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

Which are 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 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:

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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".