NDC 69423-434 Secret Honeysuckle Clear

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:
69423-434
Proprietary Name:
Secret Honeysuckle Clear
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]
01-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69423-434-73

Package Description: 73 g in 1 CYLINDER

Product Details

What is NDC 69423-434?

The NDC code 69423-434 is assigned by the FDA to the product Secret Honeysuckle Clear which is product labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69423-434-73 73 g in 1 cylinder . 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 Secret Honeysuckle Clear?

Apply to underarms onlyapply 2-3 clicks as needed

Which are Secret Honeysuckle Clear UNII Codes?

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

  • ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY)
  • ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (Active Moiety)

Which are Secret Honeysuckle Clear 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".