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NDC 70042-0002 Recovery

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70042-0002?
  4. Recovery 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:
70042-0002
Proprietary Name:
Recovery
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Powerful X
Labeler Code:
70042
Product Label ID:
6a2dea96-b06e-0f68-e053-2991aa0ad34c
Start Marketing Date: [9]
04-19-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 70042-0002?

The NDC code 70042-0002 is assigned by the FDA to the product Recovery which is product labeled by Powerful X. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 70042-0002-1 500 ml in 1 bottle, pump , 70042-0002-2 250 ml in 1 tube , 70042-0002-3 100 ml in 1 tube , 70042-0002-4 60 ml in 1 tube , 70042-0002-5 30 ml in 1 tube , 70042-0002-6 2 ml in 1 jar . 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 Recovery?

Use Pre- Activity: Put on the FlexPower recovery cream and massage your body parts for 10 minutes to warm up before doing exercises. No matter what purpose of the workout is, applyting FlexPower can help to warm-up your body and deliver a better time of exercising. Use After-Activty: After Applied- Use the FlexPower recovery cream as a lotion and massage when applying for warm-sensation after shower. Wash your hand with soap after application.

Which are Recovery UNII Codes?

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

Which are Recovery 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:

* Please review the disclaimer below.

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".