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  4. NDC Product Code: 27495-025 Overtime-hmp

NDC 27495-025 Overtime-hmp

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 27495-025?
  4. Overtime-hmp 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:
27495-025
Proprietary Name:
Overtime-hmp
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Science And Nature, Inc.
Labeler Code:
27495
Product Label ID:
ceade408-adc7-1ba2-e053-2a95a90ae0cc
Start Marketing Date: [9]
11-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 27495-025?

The NDC code 27495-025 is assigned by the FDA to the product Overtime-hmp which is product labeled by Physicians Science And Nature, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 27495-025-02 72 g 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 Overtime-hmp?

Consult a physician prior to use. Use only as directed. Prior to first use, rub a small amount on the forearm to check for sensitivity. Gently rub over painful areas no more than 4 times daily. Do not massage into skin vigorously. Wash hands thoroughly after each use. If place into eyes, rinse with cold water and call for medical help.

Which are Overtime-hmp UNII Codes?

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

Which are Overtime-hmp 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".