NDC 54340-682 Dry Idea Ad Antiperspirant Roll-on Powder Fresh

NDC Product Code 54340-682

NDC 54340-682-01

Package Description: 96.1 mL in 1 BOTTLE, WITH APPLICATOR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Dry Idea Ad Antiperspirant Roll-on Powder Fresh with NDC 54340-682 is a product labeled by The Dial Corporation. The generic name of Dry Idea Ad Antiperspirant Roll-on Powder Fresh is . The product's dosage form is and is administered via form.

Labeler Name: The Dial Corporation

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: The Dial Corporation
Labeler Code: 54340
Start Marketing Date: 05-21-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Dry Idea Ad Antiperspirant Roll-on Powder Fresh Product Label Images

Dry Idea Ad Antiperspirant Roll-on Powder Fresh Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Aluminum Zirconium Pentachlorohydrex Gly 16.3%

Otc - Purpose

USE:  Reduces underarm perspiration.  Extra effective

Warnings

Warnings.....For external use only.

Otc - Do Not Use

Do not use on broken skin.

Otc - Stop Use

Stop use and ask a doctor is rash or irritation occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease.

Indications & Usage

Directions:  Shake well.  Apply to underarms only.

Inactive Ingredient

Inactive Ingredients:  Cyclomethicone, Disteardimonium Hectorite, Propylene Carbonate, Gossypium Herbaceum (Cotton) Seed Oil, Tocopheryl Acetate (Vitamin E Acetate), Isopropyl Myristate, Fragrance, Zea Mays (Corn) Starch.

Otc - Questions

Questions:  1-800-258-DIAL

How Supplied

2009 Distributed By The Dial Corporation, A Henkel Company, Scottsdale, AZ 85255.  The distinctive design and elements of this package ae proprietary and owned by the Dial Corporation, A Henkel Company.

Dosage & Administration

DIRECTIONS: Shake well. Apply to underarms only.

* Please review the disclaimer below.