Label: DERMAL WOUND CLEANSER- benzethonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 69740-490-00, 69740-492-00 - Packager: Smith & Nephew Medical Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 20, 2020
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PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - DERMAL WOUND CLEANSER BOTTLE, SPRAY (473 mL)
Smith&Nephew
REF 449000
NDC 69740-490-00Dermal
Wound
CleanserFirst Aid Antiseptic
- Helps reduce risk of infection in wounds and burns
- Gentle wound cleansing
- Safe and easy to use
- pH-buffered
- Non-irritating
16 fl. oz. (473 mL)
Made in the USA for Smith & Nephew Medical Ltd.
101 Hessle Road
Hull
HU3 2BN
England
www.smith-nephew.com -
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - DERMAL WOUND CLEANSER BOTTLE, SPRAY (236 mL)
Smith&Nephew
#59449200
NDC 69740-492-00
Dermal
Wound
CleanserFirst Aid Antiseptic
- Helps reduce risk of infection in wounds and burns
- Gentle wound cleansing
- Safe and easy to use
- pH-buffered
- Non-irritating
8 fl. oz. (236 mL)
Made in the USA for Smith & Nephew Medical Ltd.
101 Hessle Road
Hull
HU3 2BN
England
www.smith-nephew.com -
INGREDIENTS AND APPEARANCE
DERMAL WOUND CLEANSER
benzethonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69740-490 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 1.3 g in 981 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) WATER (UNII: 059QF0KO0R) SODIUM CITRATE (UNII: 1Q73Q2JULR) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69740-490-00 473 mL in 1.0 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/1994 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/1994 DERMAL WOUND CLEANSER
benzethonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69740-492 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 1.3 g in 981 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM CITRATE (UNII: 1Q73Q2JULR) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69740-492-00 236 mL in 1.0 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/1991 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/1991 Labeler - Smith & Nephew Medical Ltd. (216344051) Establishment Name Address ID/FEI Business Operations Swiss-American CDMO, LLC 080170933 MANUFACTURE(69740-490, 69740-492) , analysis(69740-490, 69740-492) , pack(69740-490, 69740-492)