NDC 59779-577 Cvs Effervescent Pain Relief Pm

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:
59779-577
Proprietary Name:
Cvs Effervescent Pain Relief Pm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
59779
Start Marketing Date: [9]
02-02-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
15 MM
Imprint(s):
RP177
Score:
1
Flavor(s):
BERRY (C73365)

Code Structure Chart

Product Details

What is NDC 59779-577?

The NDC code 59779-577 is assigned by the FDA to the product Cvs Effervescent Pain Relief Pm which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-577-16 16 tablet in 1 carton . 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 Cvs Effervescent Pain Relief Pm?

•do not take more than directed (see Overdose warning)•dissolve tablets fully in 8 oz of water at room temperature•do not chew or swallow tabletAdults and children 12 years and over •take 2 tablets fully dissolved in 8 oz of water at room temperature at bedtime•do not take more than 2 tablets in 24 hourschildren under 12 yearsdo not use

Which are Cvs Effervescent Pain Relief Pm UNII Codes?

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

Which are Cvs Effervescent Pain Relief Pm 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".