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  4. NDC Product Code: 71718-111 Biotemper

NDC 71718-111 Biotemper

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71718-111?
  4. Biotemper Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71718-111
Proprietary Name:
Biotemper
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Scientific Solutions Global Llc
Labeler Code:
71718
Product Label ID:
1486c893-ec00-4603-93fd-01f68b7e0b81
Start Marketing Date: [9]
08-03-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71718-111-01

Package Description: 89 mL in 1 BOTTLE

NDC Code 71718-111-02

Package Description: 2 BOTTLE in 1 PACKAGE / 89 mL in 1 BOTTLE

NDC Code 71718-111-03

Package Description: 3 BOTTLE in 1 PACKAGE / 89 mL in 1 BOTTLE

NDC Code 71718-111-04

Package Description: 4 BOTTLE in 1 PACKAGE / 89 mL in 1 BOTTLE

NDC Code 71718-111-05

Package Description: 6 BOTTLE in 1 PACKAGE / 89 mL in 1 BOTTLE

NDC Code 71718-111-06

Package Description: 12 BOTTLE in 1 PACKAGE / 89 mL in 1 BOTTLE

Product Details

What is NDC 71718-111?

The NDC code 71718-111 is assigned by the FDA to the product Biotemper which is product labeled by Scientific Solutions Global Llc. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 71718-111-01 89 ml in 1 bottle , 71718-111-02 2 bottle in 1 package / 89 ml in 1 bottle, 71718-111-03 3 bottle in 1 package / 89 ml in 1 bottle, 71718-111-04 4 bottle in 1 package / 89 ml in 1 bottle, 71718-111-05 6 bottle in 1 package / 89 ml in 1 bottle, 71718-111-06 12 bottle in 1 package / 89 ml in 1 bottle. 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 Biotemper?

• Adults and children 2 years of age and older: Apply to affected area not more than 4 times daily in one direction, not circular. • Children under 2 years of age, consult a physician • Massage not necessary • Shake well before use

Which are Biotemper UNII Codes?

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

Which are Biotemper 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 Biotemper?

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.

[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".