Benzalkonium Chloride
Dial Gold Soap
The Original Bradford Soap Works Inc
Human Otc Drug
NDC 11118-0011Benzalkonium Chloride also known as Dial Gold Soap is a human otc drug labeled by 'The Original Bradford Soap Works Inc'. National Drug Code (NDC) number for Benzalkonium Chloride is 11118-0011. This drug is available in dosage form of Soap. The names of the active, medicinal ingredients in Benzalkonium Chloride drug includes Benzalkonium Chloride - .113 g/113g . The currest status of Benzalkonium Chloride drug is Active.
Drug Information:
| Drug NDC: | 11118-0011 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Benzalkonium Chloride |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Dial Gold Soap |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | The Original Bradford Soap Works Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Soap |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | BENZALKONIUM CHLORIDE - .113 g/113g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 01 Jul, 2017 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 23 Jun, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part333A |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | The Original Bradford Soap Works Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1926450
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | F5UM2KM3W7
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 11118-0011-1 | 339 g in 1 CELLO PACK (11118-0011-1) | 01 Jul, 2017 | N/A | No |
| 11118-0011-2 | 554 g in 1 CELLO PACK (11118-0011-2) | 01 Jul, 2017 | N/A | No |
| 11118-0011-3 | 452 g in 1 CELLO PACK (11118-0011-3) | 01 Jul, 2017 | N/A | No |
| 11118-0011-4 | 678 g in 1 CELLO PACK (11118-0011-4) | 01 Jul, 2017 | N/A | No |
| 11118-0011-5 | 181 g in 1 CELLO PACK (11118-0011-5) | 01 Jul, 2017 | N/A | No |
| 11118-0011-6 | 1356 g in 1 CELLO PACK (11118-0011-6) | 01 Jul, 2017 | N/A | No |
| 11118-0011-7 | 1130 g in 1 CELLO PACK (11118-0011-7) | 01 Jul, 2017 | N/A | No |
| 11118-0011-8 | 904 g in 1 PACKAGE (11118-0011-8) | 01 Jul, 2017 | N/A | No |
| 11118-0011-9 | 637 g in 1 CELLO PACK (11118-0011-9) | 01 Jul, 2017 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Antibacterial
Product Elements:
Benzalkonium chloride dial gold soap benzalkonium chloride benzalkonium sodium tallowate, beef
Indications and Usage:
Washing to decrease bacteria on skin
Warnings:
For external use only. when using this product avoid contact with eyes. in case of eye contact, flush with water.
Dosage and Administration:
Wet bar with water. lather vigorously and wash skin. rinse and dry thoroughly.
Package Label Principal Display Panel:
Henkel ®, tm, ©2018 distributed by henkel corporation, rocky hill, ct 06067 2342055 dial complete ® gold antibacterial eliminates 99% of bacteria** clean rinsing, non-drying deodorant bar soap â round the clock* odor protection skin smart formulas from dial® are created with moisturizing conditioners & gentle cleansers to give you a balanced clean. 2708589 #1 antibacterial bar soap band+ dial complete® gold antibacterial eliminates 99% of bacteria** clean rinsing, non-drying deodorant bar soap skin smart 2-3.2 oz soap bars (90g) each total net wt 64oz (180g) 2 bars moisturizing conditioners gentle cleansers free from parabens, phthalates, silicones #1 antibacterial bar soap band+ dial complete® gold antibacterial eliminates 99% of bacteria** clean rinsing, non-drying deodorant bar soap skin smart 2-3.2 oz soap bars (90g) each total net wt 64oz (180g) 2 bars moisturizing conditioners gentle cleansers free from parabens, phthalates, silicones drug facts active ingredient purpose benzalkonium chloride 0.10%..........antibacterial uses for washing to decrease bacteria on the skin warnings 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 if irritation and redness develops keep out of reach of children. if swallowed, get medical help or contact a poison control center right away. directions: wet bar with water. lather vigorously and wash skin. rinse and dry thoroughly. inactive ingredients: soap (sodium tallowate* ⢠sodium palmate*â¢sodium cocoate*⢠sodium palm kernelate)⢠water ⢠glycerin ⢠coconut acid* ⢠palm acid ⢠palm kernel acid* ⢠stearic acid * ⢠tallow acid * ⢠sodium chloride ⢠fragrance ⢠peg-6 methyl ether ⢠pentasodium pentetate ⢠tetrasodium etidronate ⢠yellow 5 ⢠titanium dioxide ⢠alcohol ⢠yellow 8 ⢠red 4 *contains one or more of these ingredients questions? 1-800-258-dial (3425) +based on iri mulo unit sales data for the 52 week period ending 2/18/21. **in a 30 second wash test vs. s. marcescens visit our website at www.dialsoap.com henkel®, tm, ©2021 distributed by henkel corporation, rocky hill ct 06067 outer wrapper