NDC 76176-037 Invisible Solid Anti-perspirant And Deodorant

Aluminum Chlorohydrate Gel

NDC Product Code 76176-037

NDC CODE: 76176-037

Proprietary Name: Invisible Solid Anti-perspirant And Deodorant 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

  • 76176 - Ningbo Liyuan Daily Chemical Products Co., Ltd.
    • 76176-037 - Invisible Solid Anti-perspirant And Deodorant

NDC 76176-037-01

Package Description: 64 g in 1 TUBE

NDC Product Information

Invisible Solid Anti-perspirant And Deodorant with NDC 76176-037 is a a human over the counter drug product labeled by Ningbo Liyuan Daily Chemical Products Co., Ltd.. The generic name of Invisible Solid Anti-perspirant And Deodorant is aluminum chlorohydrate gel. The product's dosage form is stick and is administered via topical form.

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.

Invisible Solid Anti-perspirant And Deodorant 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.


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.

  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • PEG-8 DISTEARATE (UNII: 7JNC8VN07M)

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: Ningbo Liyuan Daily Chemical Products Co., Ltd.
Labeler Code: 76176
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: 01-01-2016 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".

* Please review the disclaimer below.

Invisible Solid Anti-perspirant And Deodorant Product Label Images

Invisible Solid Anti-perspirant And Deodorant 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 Ingredients

Aluminum Chlorohydrates 20%

Purpose

Antiperspirant

Use

Reduces underarm wetness and perspiration.

Warnings

For external use only

Do Not Use

On broken or irritated skin.

Stop Use And Ask A Doctor

If irritation or rash develops.

Keep Out Of Reach Of Children.

If swallowed, seek medical help or contact a Posion Control Center immediately.

Directions

Remove cap, turn dial to raise product, apply envely to underarms only, replace cap after use.

Inactive Ingredients

Mineral Oil, Stearic Acid, Stearyl Alcohol, Cyclopentasiloxane, Isopropyl Palmitate, Hydrogenated Castor Oil, Fragrance, Silica, PEG-8 Distearate, BHT

* Please review the disclaimer below.