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  4. NDC Product Code: 53807-220 Infants Pain Reliever

NDC 53807-220 Infants Pain Reliever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53807-220?
  5. Infants Pain Reliever 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:
53807-220
Proprietary Name:
Infants Pain Reliever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rij Pharmaceutical Corporation
Labeler Code:
53807
Product Label ID:
d78154b6-b3f0-4ad8-8f83-ccc6c2df770b
Start Marketing Date: [9]
03-16-1999
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 53807-220?

The NDC code 53807-220 is assigned by the FDA to the product Infants Pain Reliever which is product labeled by Rij Pharmaceutical Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53807-220-05 1 bottle, plastic in 1 carton / 15 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 Infants Pain Reliever?

This product does not contain directions or complete warnings for adult use.shake well before usingfind right dose on chart below. If possible, use weight to dose; otherwise, use age.fill to dose level. Do not use any other dosing device.dispense liquid slowly into child's mouth, toward inner cheek.if needed, repeat dose every 4 hours while symptoms last.do not give use than 5 times in 24 hoursreplace original bottle cap to maintain child resistanceuse only with enclosed dropperrinse dropper after each useDosing ChartWeight (lbs.)Age (yrs.)Dose ( mL) under 24under 2ask a doctor24-352-32 droppersful (0.8 + 0.8 mL)Attention: Specifically designed for use with enclosed dropper. Use only enclosed dropper to dose this product. Do not use any other dosing devices.

Which are Infants Pain Reliever UNII Codes?

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

Which are Infants Pain Reliever 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 Infants Pain Reliever?

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".