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  4. NDC Product Code: 79170-001 Straight Shot

NDC 79170-001 Straight Shot

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79170-001?
  4. Straight Shot 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:
79170-001
Proprietary Name:
Straight Shot
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shift Packaging, Llc
Labeler Code:
79170
Product Label ID:
0fa7304a-e8e4-4f33-a92b-43c772432e67
Start Marketing Date: [9]
11-05-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79170-001-01

Package Description: 3785 mL in 1 PACKAGE

Product Details

What is NDC 79170-001?

The NDC code 79170-001 is assigned by the FDA to the product Straight Shot which is product labeled by Shift Packaging, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79170-001-01 3785 ml in 1 package . 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 Straight Shot?

■ hold sprayer tip away from face when opening.■ clean affected area.■ if bandaged,let dry first. ■ may be covered with a stenile bandage.■ apply a small amount of product on affected area 1-3 times a day.

Which are Straight Shot UNII Codes?

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

Which are Straight Shot 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 Straight Shot?

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".