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  4. NDC Product Code: 21695-065 Ibuprofen (nsaid) Pain Releiver/ Fever Reducer

NDC 21695-065 Ibuprofen (nsaid) Pain Releiver/ Fever Reducer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 21695-065?
  5. Ibuprofen (nsaid) Pain Releiver/ 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:
21695-065
Proprietary Name:
Ibuprofen (nsaid) Pain Releiver/ Fever Reducer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp
Labeler Code:
21695
Product Label ID:
7b4858fc-fea6-4e4c-886e-a2febe1ed2c3
Start Marketing Date: [9]
12-16-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
IP;140
Score:
1

Code Structure Chart

Product Details

What is NDC 21695-065?

The NDC code 21695-065 is assigned by the FDA to the product Ibuprofen (nsaid) Pain Releiver/ Fever Reducer which is product labeled by Rebel Distributors Corp. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 21695-065-06 6 tablet in 1 bottle , 21695-065-14 14 tablet in 1 bottle , 21695-065-28 28 tablet in 1 bottle , 21695-065-30 30 tablet in 1 bottle , 21695-065-50 50 tablet in 1 bottle , 21695-065-60 60 tablet in 1 bottle , 21695-065-90 90 tablet 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 Ibuprofen (nsaid) Pain Releiver/ Fever Reducer?

Do not take more than directedthe smallest effective dose should be usedAdults and children12 years and oldertake 1 tablet every 4 to 6 hours while symptoms persistif pain or fever does not respond to 1 tablet, 2 tablets may be useddo not exceed 6 tablets in 24 hours, unless directed by a doctorChildren under 12 yearsask a doctor

Which are Ibuprofen (nsaid) Pain Releiver/ Fever Reducer UNII Codes?

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

Which are Ibuprofen (nsaid) Pain Releiver/ 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 Ibuprofen (nsaid) Pain Releiver/ 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".