NDC 69423-449 Old Spice Gentleman S Blend Mandarin And Musk

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:
69423-449
Proprietary Name:
Old Spice Gentleman S Blend Mandarin And Musk
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Procter & Gamble Manufacturing Company
Labeler Code:
69423
Start Marketing Date: [9]
01-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69423-449-01

Package Description: 1 CANISTER in 1 CARTON / 73 g in 1 CANISTER

NDC Code 69423-449-73

Package Description: 73 g in 1 CANISTER

Product Details

What is NDC 69423-449?

The NDC code 69423-449 is assigned by the FDA to the product Old Spice Gentleman S Blend Mandarin And Musk which is product labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69423-449-01 1 canister in 1 carton / 73 g in 1 canister, 69423-449-73 73 g in 1 canister . 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 Old Spice Gentleman S Blend Mandarin And Musk?

Apply to underarms only

Which are Old Spice Gentleman S Blend Mandarin And Musk UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)

Which are Old Spice Gentleman S Blend Mandarin And Musk 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".