NDC 81238-0560 Aramark Pain-free Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
81238-0560
Proprietary Name:
Aramark Pain-free Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
81238
Start Marketing Date: [9]
05-07-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
FR9
Score:
1

Code Structure Chart

Product Details

What is NDC 81238-0560?

The NDC code 81238-0560 is assigned by the FDA to the product Aramark Pain-free Extra Strength which is product labeled by Western First Aid Safety Dba Aramark. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 81238-0560-2 50 packet in 1 box / 2 tablet in 1 packet, 81238-0560-3 125 packet in 1 box / 2 tablet in 1 packet. 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 Aramark Pain-free Extra Strength?

Uses:Temporarily Relieves minor aches and painsassociated with: • backach • headaches• colds • toothache • minor arthritis pain• muscular aches • menstrual cramps

Which are Aramark Pain-free Extra Strength UNII Codes?

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

Which are Aramark Pain-free Extra Strength 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 Aramark Pain-free Extra Strength?

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:
  • RxCUI: 308297 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet
  • RxCUI: 308297 - APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet

* Please review the disclaimer below.

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".