NDC 52904-841 Midol Complete

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:
52904-841
Proprietary Name:
Midol Complete
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Select Corporation
Labeler Code:
52904
Start Marketing Date: [9]
02-10-2014
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
MIDOL
Score:
1

Product Packages

NDC Code 52904-841-04

Package Description: 1 POUCH in 1 BLISTER PACK / 2 TABLET in 1 POUCH

NDC Code 52904-841-20

Package Description: 20 POUCH in 1 CARTON / 2 TABLET in 1 POUCH

NDC Code 52904-841-25

Package Description: 25 POUCH in 1 CARTON / 2 TABLET in 1 POUCH

NDC Code 52904-841-30

Package Description: 30 POUCH in 1 CARTON / 2 TABLET in 1 POUCH

Product Details

What is NDC 52904-841?

The NDC code 52904-841 is assigned by the FDA to the product Midol Complete which is product labeled by Select Corporation. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 52904-841-04 1 pouch in 1 blister pack / 2 tablet in 1 pouch, 52904-841-20 20 pouch in 1 carton / 2 tablet in 1 pouch, 52904-841-25 25 pouch in 1 carton / 2 tablet in 1 pouch, 52904-841-30 30 pouch in 1 carton / 2 tablet in 1 pouch. 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 Midol Complete?

Do not take more than the recommended doseadults and children 12 years and oldertake 2 caplets with waterrepeat every 6 hours, as needed do not exceed 6 caplets per daychildren under 12 yearsconsult a doctor

Which are Midol Complete UNII Codes?

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

Which are Midol Complete 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 Midol Complete?

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: 1597298 - acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet
  • RxCUI: 1597298 - APAP 500 MG / Caffeine 60 MG / Pyrilamine Maleate 15 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".