Label: DI-DAK-SOL- sodium hypochlorite solution
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Contains inactivated NDC Code(s)
NDC Code(s): 0436-0669-16 - Packager: Century Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 7, 2019
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
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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 surrounding intact skin with a moisture
barrier ointment or skin sealant as needed.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DI-DAK-SOL
sodium hypochlorite solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0436-0669 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) SODIUM HYPOCHLORITE 0.125 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:0436-0669-16 473 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 02/05/2001 Labeler - Century Pharmaceuticals, Inc. (042815464) Establishment Name Address ID/FEI Business Operations Century Pharmaceuticals, Inc. 042815464 pack(0436-0669) , analysis(0436-0669) , manufacture(0436-0669) , label(0436-0669)