NDC 66715-9799 Nodoz Alertness Aid Maximum 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:
66715-9799
Proprietary Name:
Nodoz Alertness Aid Maximum Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
66715
FDA Application Number: [6]
part340
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
12-07-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
NODOZ
Score:
2

Code Structure Chart

Product Details

What is NDC 66715-9799?

The NDC code 66715-9799 is assigned by the FDA to the product Nodoz Alertness Aid Maximum Strength which is product labeled by Lil' Drug Store Products, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 66715-9799-0 10 tablet, film coated in 1 vial, plastic , 66715-9799-2 2 pouch in 1 carton / 2 tablet, film coated in 1 pouch, 66715-9799-3 3 pouch in 1 carton / 2 tablet, film coated in 1 pouch, 66715-9799-4 2 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack, 66715-9799-6 1 bottle, plastic in 1 carton / 60 tablet, film coated in 1 bottle, plastic. 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 Nodoz Alertness Aid Maximum Strength?

Adults and children 12 years of age and over:take 1/2 to 1 caplet not more often than every 3 to 4 hours

Which are Nodoz Alertness Aid Maximum Strength UNII Codes?

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

Which are Nodoz Alertness Aid Maximum 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 Nodoz Alertness Aid Maximum 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:

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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".