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  4. NDC Product Code: 74306-134 Guardrx Lavender Peppermint Extra Strength

NDC 74306-134 Guardrx Lavender Peppermint Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74306-134?
  4. Guardrx Lavender Peppermint Extra Strength 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:
74306-134
Proprietary Name:
Guardrx Lavender Peppermint Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gps Associates
Labeler Code:
74306
Product Label ID:
a4874b8b-d4ce-dbcc-e053-2995a90afcb7
Start Marketing Date: [9]
05-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74306-134?

The NDC code 74306-134 is assigned by the FDA to the product Guardrx Lavender Peppermint Extra Strength which is product labeled by Gps Associates. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 74306-134-02 59 ml in 1 bottle, spray , 74306-134-04 118 ml in 1 bottle, spray , 74306-134-08 236 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 Guardrx Lavender Peppermint Extra Strength?

Wet hands thoroughly with product and allow to dry without wiping.-Do not use other than directed. Wet hands thoroughly with product and allow to dry without wiping.-Do not use other than directed. Wet hands thoroughly with product and allow to dry without wiping.-Do not use other than directed.

Which are Guardrx Lavender Peppermint Extra Strength UNII Codes?

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

Which are Guardrx Lavender Peppermint Extra Strength 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".