NDC 74306-135 Guardrx Unscented Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
74306-135
Proprietary Name:
Guardrx Unscented Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gps Associates
Labeler Code:
74306
Start Marketing Date: [9]
05-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74306-135-02

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Code 74306-135-04

Package Description: 118 mL in 1 BOTTLE, SPRAY

NDC Code 74306-135-08

Package Description: 236 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 74306-135?

The NDC code 74306-135 is assigned by the FDA to the product Guardrx Unscented 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 74306-135-02 59 ml in 1 bottle, spray , 74306-135-04 118 ml in 1 bottle, spray , 74306-135-08 236 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 Unscented 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 Unscented Extra Strength UNII Codes?

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

Which are Guardrx Unscented 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:

What is the NDC to RxNorm Crosswalk for Guardrx Unscented Extra Strength?

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".