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  4. NDC Product Code: 11673-160 Up And Up Juniors Acetaminophen

NDC 11673-160 Up And Up Juniors Acetaminophen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 11673-160?
  5. Up And Up Juniors 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:
11673-160
Proprietary Name:
Up And Up Juniors Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Product Label ID:
72804e03-4043-4188-85ac-9272f13856a3
Start Marketing Date: [9]
10-19-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327)
Shape:
ROUND (C48348)
Size(s):
16 MM
Imprint(s):
RP160
Score:
2
Flavor(s):
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 11673-160?

The NDC code 11673-160 is assigned by the FDA to the product Up And Up Juniors Acetaminophen which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 11673-160-31 4 blister pack in 1 carton / 6 tablet, chewable in 1 blister pack, 11673-160-32 4 blister pack in 1 carton / 6 tablet, chewable in 1 blister 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 Up And Up Juniors Acetaminophen?

•this product does not contain directions or complete warnings for adult use.•do not give more than directed (see overdose warning)•find the right dose on chart below. If possible, use weight to dose; otherwise use age. •dissolve in mouth or chew before swallowing •if needed, repeat dose every 4 hours while symptoms last •do not give more than 5 times in 24 hours •do not give for more than 5 days unless directed by a doctorWeight (lb)under 4848-5960-7172-9596 and overAge (yr)under 6 years6-8 years 9-10 years11 years12 yearsTablets ask a doctor 22 1/234

Which are Up And Up Juniors Acetaminophen UNII Codes?

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

Which are Up And Up Juniors 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 Up And Up Juniors 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".