NDC 69365-004 Facol Cold And Flu Day And Night

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:
69365-004
Proprietary Name:
Facol Cold And Flu Day And Night
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jw Holdings
Labeler Code:
69365
Start Marketing Date: [9]
08-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - SOFT LIQUID FILLED CAPSULE)
BLUE (C48333 - SOFT LIQUID FILLED CAPSULE)
Shape:
CAPSULE (C48336)
Size(s):
20 MM
Imprint(s):
FDFN
Score:
1

Product Packages

NDC Code 69365-004-01

Package Description: 1 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Product Details

What is NDC 69365-004?

The NDC code 69365-004 is assigned by the FDA to the product Facol Cold And Flu Day And Night which is product labeled by Jw Holdings. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69365-004-01 1 blister pack in 1 carton / 1 capsule, liquid filled 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 Facol Cold And Flu Day And Night?

■ Do not take more than directed■ children under 15 years: ask a doctor ■ adults and children 15 years and over: take 2 daytime capsules 2 times a day ■ Take 2 nighttime capsules before sleep ■ do not take nighttime capsule and daytime capsule together

Which are Facol Cold And Flu Day And Night UNII Codes?

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

Which are Facol Cold And Flu Day And Night 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:

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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".