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  4. NDC Product Code: 59332-001 Sprayable Energy

NDC 59332-001 Sprayable Energy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59332-001?
  4. Sprayable Energy Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59332-001
Proprietary Name:
Sprayable Energy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Spayable Energy Llc
Labeler Code:
59332
Product Label ID:
5c5140fa-f1a2-4db6-999b-ffecf692e81a
Start Marketing Date: [9]
08-20-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59332-001-08

Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 8 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 59332-001?

The NDC code 59332-001 is assigned by the FDA to the product Sprayable Energy which is product labeled by Spayable Energy Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59332-001-08 1 bottle, spray in 1 carton / 8 ml in 1 bottle, spray. 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 Sprayable Energy?

Adults over 18 years of age: twist bottle open and spray 4 times on your neck (twice on each side) not more than 6 times per daydo not exceed 24 sprays in 24 hoursadults and children under 18 years of age: consult a physician

Which are Sprayable Energy UNII Codes?

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

Which are Sprayable Energy 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".