NDC 64942-1846 Dove

Men Skin Defense Antibacterial 3n1 Hand Body Shave Bar

NDC Product Code 64942-1846

NDC 64942-1846-1

Package Description: 212 g in 1 CARTON

NDC 64942-1846-2

Package Description: 425 g in 1 CARTON

NDC 64942-1846-3

Package Description: 637 g in 1 CARTON

NDC Product Information

Dove with NDC 64942-1846 is a a human over the counter drug product labeled by Conopco Inc. D/b/a/ Unilever. The generic name of Dove is men skin defense antibacterial 3n1 hand body shave bar. The product's dosage form is soap and is administered via topical form.

Labeler Name: Conopco Inc. D/b/a/ Unilever

Dosage Form: Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.

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.

Dove 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.

  • BENZALKONIUM CHLORIDE .13 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.

  • SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)
  • SODIUM OLEATE (UNII: 399SL044HN)
  • SODIUM STEARATE (UNII: QU7E2XA9TG)
  • SODIUM ISETHIONATE (UNII: 3R36J71C17)
  • LAURIC ACID (UNII: 1160N9NU9U)
  • SODIUM LAURATE (UNII: K146MR5EXO)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
  • KAOLIN (UNII: 24H4NWX5CO)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • WATER (UNII: 059QF0KO0R)
  • EDETATE SODIUM (UNII: MP1J8420LU)

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: Conopco Inc. D/b/a/ Unilever
Labeler Code: 64942
FDA Application Number: part333A 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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 01-15-2021 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: 12-31-2022 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.

Dove 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

Dove Men +Care Skin Defense Antibacterial 3-N-1 Hand + Body + Shave Bar - Benzalkonium Chloride Soap

Dove Men +Care Skin Defense Antibacterial 3-N-1 Hand + Body + Shave Bar

Drug Facts

Active ingredientBenzalkonium Chloride (0.13%)

Purpose

Antibacterial

Uses

For washing to decrease bacteria on the skin

Warnings

• For external use only

• When using this product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with wate
r

• Stop use and ask doctor
if irritation or redness develop.

Otc - Keep Out Of Reach Of Children

• Keep out of reach of children except under adult supervision.If swallowed, get medical help or contact a poison control Center right away.

Directions

Wet bar with water, lather vigorously and use all over body. Rinse clean.

Inactive Ingredients

Sodium Lauroyl Isethionate, Stearic Acid, Sodium Oleate, Sodium Stearate, Water (Aqua), Sodium Isethionate, Lauric Acid, Sodium C14-16 Olefin Sulfonate, Sodium Laurate, Fragrance (Parfum), Dipropylene Glycol, Sodium Chloride, Tetrasodium Etidronate, Tetrasodium EDTA, Kaolin*, Titanium Dioxide*, Yellow 5 (CI 19140), Yellow 6 (CI 15985). *Contains one or more of these ingredients

* Please review the disclaimer below.