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  4. NDC Product Code: 63029-075 Pediacare Single Dose Fever Reducer

NDC 63029-075 Pediacare Single Dose Fever Reducer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63029-075?
  5. Pediacare Single Dose Fever Reducer 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:
63029-075
Proprietary Name:
Pediacare Single Dose Fever Reducer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medtech Products Inc.
Labeler Code:
63029
Product Label ID:
6032dc92-44e5-4f32-b1a6-bba6695d2dcc
Start Marketing Date: [9]
05-15-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 63029-075?

The NDC code 63029-075 is assigned by the FDA to the product Pediacare Single Dose Fever Reducer which is product labeled by Medtech Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63029-075-07 7 dose pack in 1 box, unit-dose / 7.5 ml in 1 dose pack. 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 Pediacare Single Dose Fever Reducer?

•       This product does not contain directions or complete warnings for adult use.•       Each packet provides 1 dose for a child who is 48 to 59 pounds or 6 to 8 years of age. If possible, use weight to determine dose; otherwise use age.To use:•       Fold back at the dotted line to reveal the tear strip.•       Tear across (not up & down) at the exposed tear slit•       Remove and discard strip•       Squeeze medicine into child’s mouth.•       If needed, repeat dose every 4 hours while symptoms last.•       Do not give more than 5 times in 24 hours (see overdose warning).•       Do not give more than 5 days unless directed by a doctor. •       This product does not contain directions or complete warnings for adult use.•       Each packet provides 1 dose for a child who is 36 to 47 pounds or 4 to 5 years of age. If possible, use weight to determine dose; otherwise use age.To use:•       Fold back at the dotted line to reveal the tear strip.•       Tear across (not up & down) at the exposed tear slit•       Remove and discard strip•       Squeeze medicine into child’s mouth.•       If needed, repeat dose every 4 hours while symptoms last.•       Do not give more than 5 times in 24 hours (see overdose warning).•       Do not give more than 5 days unless directed by a doctor.

Which are Pediacare Single Dose Fever Reducer UNII Codes?

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

Which are Pediacare Single Dose Fever Reducer 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 Pediacare Single Dose Fever Reducer?

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".