NDC 69517-103 Nighttime Cold And Flu Relief

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:
69517-103
Proprietary Name:
Nighttime Cold And Flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Healthlife Of Usa
Labeler Code:
69517
Start Marketing Date: [9]
08-26-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
CAPSULE (C48336)
Size(s):
22 MM
Imprint(s):
215
Score:
1

Product Packages

NDC Code 69517-103-10

Package Description: 1 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 69517-103-16

Package Description: 16 CAPSULE, LIQUID FILLED in 1 BOTTLE

Product Details

What is NDC 69517-103?

The NDC code 69517-103 is assigned by the FDA to the product Nighttime Cold And Flu Relief which is product labeled by Healthlife Of Usa. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69517-103-10 1 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack, 69517-103-16 16 capsule, liquid filled 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 Nighttime Cold And Flu Relief?

This product is used as Pain reliever/fever reducerCough suppressantAntihistamine. Temporarily relieves common cold and flu symptoms: cough due to minor throat and bronchial irritation sore throat headache minor aches and pains feverrunny nose and sneezing

Which are Nighttime Cold And Flu Relief UNII Codes?

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

Which are Nighttime Cold And Flu Relief 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".