NDC 69423-380 Secret Dry Rose

Aluminum Chlorohydrate

NDC Product Code 69423-380

NDC Code: 69423-380

Proprietary Name: Secret Dry Rose 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 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

  • 69423 - The Procter & Gamble Manufacturing Company
    • 69423-380 - Secret Dry Rose

NDC 69423-380-10

Package Description: 107 g in 1 CAN

NDC Product Information

Secret Dry Rose with NDC 69423-380 is a a human over the counter drug product labeled by The Procter & Gamble Manufacturing Company. The generic name of Secret Dry Rose is aluminum chlorohydrate. The product's dosage form is aerosol, spray and is administered via topical form.

Labeler Name: The Procter & Gamble Manufacturing Company

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

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.

Secret Dry Rose 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 23.5 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.

  • TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
  • BUTANE (UNII: 6LV4FOR43R)
  • 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • BETADEX (UNII: JV039JZZ3A)
  • DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)

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: The Procter & Gamble Manufacturing Company
Labeler Code: 69423
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: 07-25-2019 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.

Secret Dry Rose Product Label Images

Secret Dry Rose 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

Other

Drug Facts

Dist. by PROCTER & GAMBLE,








CINCINNATI, OH 45202.

Active Ingredient

Aluminum chlorohydrate 23.5% (anhydrous)

Purpose

Antiperspirant

Use

  • Reduces underarm wetness

Warnings

For external use only.

Otc - Do Not Use

Do not use on broken skin

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease

Otc - Stop Use

Stop use if 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.

Safe Handling Warning

Flammabledo not spray near flame or while smokingcontents under pressure

do not crush, puncture or incinerate
do not expose to heat or store at temperature above 120ºF

Otc - When Using

When using this productkeep away from face and mouth to avoid breathing itavoid spraying in eyesuse only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Directions

  • Apply to underarms only

Inactive Ingredients

Butane, hydrofluorocarbon 152A, dimethicone, fragrance, C12-15 alkyl benzoate, corn starch/maltodextrin crosspolymer, cyclodextrin, disteardimonium hectorite, mineral oil, triethyl citrate, dimethiconol.

Questions?

1-800-964-1947

* Please review the disclaimer below.

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