NDC 52904-470 Allertness Aid

NDC Product Code 52904-470

NDC CODE: 52904-470

Proprietary Name: Allertness Aid What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
WHITE (C48325 - SNOW WHITE)
Shape: ROUND (C48348)
Size(s):
11 MM
Imprint(s):
TCL363
Score: 1

NDC Code Structure

  • 52904 - Select Corporation

NDC 52904-470-02

Package Description: 2 TABLET in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Allertness Aid with NDC 52904-470 is a product labeled by Select Corporation. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 198520.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • DEXTRATES (UNII: G263MI44RU)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Select Corporation
Labeler Code: 52904
Start Marketing Date: 10-15-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Allertness Aid Product Label Images

Allertness Aid Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredients Caffeine 200mg

Otc - Purpose

Alertness Aid

Dosage & Administration

Directions: • adults and children 12 yearsand over: take 1 tablet not more often than every 3 to 4 hours

Indications & Usage

Uses: helps restore mental alertness or wakefulness whenexperiencing fatigue or drowsiness

Warnings

Warnings: Foroccasional use only. Do not use • in children under 12 yearsof age • as a substitute for sleep Caffeine warning: Therecommended dose of this product contains about as muchcaffeine as a cup of coffee. Limit the use of caffeine-containingmedications, foods, or beverages while taking this productbecause too much caffeine may cause nervousness,irritability, sleeplessness, and, occasionally, rapid heart beat.Stop use and ask a doctor if fatigue or drowsiness persists orcontinues to recur.

Otc - Pregnancy Or Breast Feeding

If pregnant orbreast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Inactive Ingredient

InactiveIngredients: carnauba wax, colloidal silicondioxide, dextrates, hypromellose, magnesium stearate,microcrystalline cellulose, polyethylene glycol, titaniumdioxide

* Please review the disclaimer below.