NDC 50663-242 Dial Complete Spring Water Fhw

Dial Complete Spring Water Fhw

NDC Product Code 50663-242

NDC 50663-242-02

Package Description: 221 mL in 1 BOTTLE, DISPENSING

NDC Product Information

Dial Complete Spring Water Fhw with NDC 50663-242 is a a human over the counter drug product labeled by Zotos International Inc. The generic name of Dial Complete Spring Water Fhw is dial complete spring water fhw. The product's dosage form is solution and is administered via topical form.

Labeler Name: Zotos International Inc

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible 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.

Dial Complete Spring Water Fhw 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.

  • WATER (UNII: 059QF0KO0R)

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.
  • 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: Zotos International Inc
Labeler Code: 50663
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: 05-01-2020 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 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.

Dial Complete Spring Water Fhw Product Label Images

Dial Complete Spring Water Fhw 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

Benzalkonium Chloride 0.13%

Active ingredient Purpose
Benzalkonium Chloride 0.13%......................................... Antibacterial




For handwashing to decrease bacteria on the skin.


For external use only.
When using this product • Avoid contact with eyes. In case of eye

contact, flush with water.

Stop Use And Ask A Doctor.

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

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.



• Pump into DRY hands

• Lather vigorously for at least 15 seconds

• Rinse and dry thoroughly

Inactive Ingredients

Inactive Ingredients: Aqua (Water, Eau) • Glycerin •

Lauramine Oxide • Cetrimonium Chloride • Cocamidopropyl Betaine •

Citric Acid • Sodium Benzoate • Hydroxypropyl Methylcellulose •

Parfum (Fragrance) • Zinc Sulfate • Sodium Chloride • Dimethyl

Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine •

CI 42090 (Blue 1) • CI 17200 (Red 33)


*Encountered in household settings

#Antibacterial Hand Soap


®,TM,©2019 Distributed by

Henkel Corporation,

Rocky Hill, CT 06067



1-800-258-DIAL (3425)

Dosage & Administration

Topical Liquid

For Handwashing To Decrease Bacteria On The Skin.

KILLS MORE BACTERIAThan Ordinary Liquid Hand Soap

* Please review the disclaimer below.