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 product labeled by The Dial Corporation. The product's dosage form is and is administered via form.

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.