NDC 69990-200 Duradry Am

Aluminum Zirconium Trichlorohydrex Glycine

NDC Product Code 69990-200

NDC 69990-200-01

Package Description: 1 CYLINDER in 1 CARTON > 65 g in 1 CYLINDER

NDC Product Information

Duradry Am with NDC 69990-200 is a a human over the counter drug product labeled by Novadore Usa, Llc. The generic name of Duradry Am is aluminum zirconium trichlorohydrex glycine. The product's dosage form is stick and is administered via topical form.

Labeler Name: Novadore Usa, Llc

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Duradry Am Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 20 g/100g

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)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ZINC RICINOLEATE (UNII: BOH1Z111J2)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Novadore Usa, Llc
Labeler Code: 69990
FDA Application Number: part350 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 01-01-2015 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: 12-31-2021 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: N - NO 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".

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Duradry Am Product Label Images

Duradry Am 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

Active Ingredient

Aluminum Zirconium Trichlorohydrex Glycine 20%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only



Stop use if rash or irritation occurs.

Do Not Use

  • On broken skin.

Ask A Doctor Before Use

If you have kidney disease

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply to underarms only.

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Dimethicone, Zinc Ricinoleate, Petrolatum, Aluminum Starch Octenylsuccinate Fragrance.

Questions?

Visit us at


www.duradry.com/amDesigned & developed by:NOVADORE USA, INCMiami, FL

* Please review the disclaimer below.