DAKINS FULL- sodium hypochlorite solution

Dakins Full by

Drug Labeling and Warnings

Dakins Full by is a Otc medication manufactured, distributed, or labeled by Century Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Hypochlorite 0.50%

PURPOSE

Antimicrobial

INDICATIONS & USAGE

Uses

To prevent and treat infections of the skin and tissue.

Pre and post surgery   Cuts, abrasions and skin ulcers

WARNINGS

For external use only.

STOP USE

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

DO NOT USE

Do not use if sensitive to chlorine compounds.

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

Directions

Pour 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 skin

with a moisture barrier ointment or skin sealant as needed.

STORAGE AND HANDLING

Other Information

Store at room temperature.

May bleach clothing.

Keep container closed when not using.

INACTIVE INGREDIENT

Purified Water, Sodium Bicarbonate, Sodium Hydroxide

QUESTIONS

Questions or Comments ?

(317) 849-4210 or 1-866-343-2576, Mon-Fri, 9AM to 4PM EST

Century Pharmaceuticals, Inc. - Indianapolis, IN 46256

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAKINS FULL 
sodium hypochlorite solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0436-0946
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N)	SODIUM HYPOCHLORITE	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0436-0946-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2006

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/08/1983

Labeler - Century Pharmaceuticals, Inc. (042815464)

Establishment
Name	Address	ID/FEI	Business Operations
Century Pharmaceuticals, Inc.		042815464	analysis(0436-0946) , label(0436-0946) , manufacture(0436-0946) , pack(0436-0946)