NDC 72197-017 2.5oz Everdry Antiperspirant Invisible

Aluminum Chlorohydrate Gel

NDC Product Code 72197-017

NDC Code: 72197-017

Proprietary Name: 2.5oz Everdry Antiperspirant Invisible What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aluminum Chlorohydrate Gel What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 72197 - American Consumer Products Corp
    • 72197-017 - 2.5oz Everdry Antiperspirant Invisible

NDC 72197-017-02

Package Description: 64 g in 1 TUBE

NDC Product Information

2.5oz Everdry Antiperspirant Invisible with NDC 72197-017 is a a human over the counter drug product labeled by American Consumer Products Corp. The generic name of 2.5oz Everdry Antiperspirant Invisible is aluminum chlorohydrate gel. The product's dosage form is stick and is administered via topical form.

Labeler Name: American Consumer Products Corp

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.

2.5oz Everdry Antiperspirant Invisible 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 CHLOROHYDRATE 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.

  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • LAURYL PALMITATE (UNII: X3V3247O54)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • ZINC (UNII: J41CSQ7QDS)
  • TALC (UNII: 7SEV7J4R1U)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)

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: American Consumer Products Corp
Labeler Code: 72197
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: 09-17-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

2.5oz Everdry Antiperspirant Invisible Product Label Images

2.5oz Everdry Antiperspirant Invisible 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

Active ingredients: Aluminum Chlorohydrate 20%

Otc - Purpose

Purpose: Antiperspirant

Warnings

Warnings: For external use only.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

Inactive Ingredient

Ingredients: Mineral Oil, Stearic Acid, Stearyl Alcohol, Zinc, Palmitate, Cyclopentasiloxane, Hydrogenated Castor Oil, Fragrance, Silica, PPG-14 Butyl Ether, PEG-8 Disterate, BHT.

Dosage & Administration

Directions: Twist base. Smooth onto dry underarms. Apply to underarms only.

Instructions For Use

Use: reduces underarm wetness and perspiration.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash develops.

Indications & Usage

Do not use on broken or irritated skin.

* Please review the disclaimer below.