NDC 0436-0946 Dakins Full

NDC Product Code 0436-0946

NDC CODE: 0436-0946

Proprietary Name: Dakins Full 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.

NDC Code Structure

  • 0436 - Century Pharmaceuticals, Inc.

NDC 0436-0946-16

Package Description: 473 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Dakins Full with NDC 0436-0946 is a product labeled by Century Pharmaceuticals, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 313049.

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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Century Pharmaceuticals, Inc.
Labeler Code: 0436
Start Marketing Date: 12-08-1983 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Dakins Full Product Label Images

Dakins Full 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

Otc - Active Ingredient

Sodium Hypochlorite 0.50%

Otc - Purpose


Indications & Usage

UsesTo prevent and treat infections of the skin and tissue.Pre and post surgery   Cuts, abrasions and skin ulcers


For external use only.

Otc - Stop Use

Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases.

Otc - Do Not Use

Do not use if sensitive to chlorine compounds.

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.

Dosage & Administration

DirectionsPour on or apply to affected area. For wound management, use as an irrigant, cleanser, or the wetting agent for a wet-to-moist dressing.Apply once daily for lightly to moderately exudative wounds.  Apply twice daily for highly exudative or highly contaminated wounds. Protect intact skinwith a moisture barrier ointment or skin sealant as needed.

Storage And Handling

Other InformationStore at room temperature.May bleach clothing.Keep container closed when not using.

Inactive Ingredient

Purified Water, Sodium Bicarbonate, Sodium Hydroxide

Otc - Questions

Questions or Comments ?(317) 849-4210 or 1-866-343-2576, Mon-Fri, 9AM to 4PM ESTCentury Pharmaceuticals, Inc. - Indianapolis, IN 46256

* Please review the disclaimer below.