Label: BEDSIDE-CARE- benzethonium chloride shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 11701-053-04, 11701-053-05 - Packager: Coloplast Corp
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 30, 2026
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- SPL UNCLASSIFIED SECTION
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Drug Facts
When using this product: do not use in the eyes, with deep or puncture wounds, serious burns, or animal bites.
Stop using this product if:
- if skin irritation and redness develop
- if condition persists for more than 7 days, consult a physician.
Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Inactive ingredients purified water, sodium lauroamphoacetate, cocamidopropyl betaine, glycerin, polysorbate 20, quaternium-52, citric acid, quaternium-15, tetrasodium EDTA.
Protocol: Rinsing is not required. Aids in the removal of urine, feces and other foreign material. Cleansing: apply to the affected area and remove with a moist washcloth. Bathing: dispense 3-4 pumps in a basin with warm water and cleanse the skin. Shampooing: pump foam directly on dampened hair, lather and remove with a moist washcloth.
Manufactured by: Coloplast A/S DK-3050 Humlebaek, Denmark
Distributed by: Coloplast Corp., Minneapolis, MN 55411 U.S.A.
1-800-533-0464 www.us.coloplast.com ©2007, Coloplast Corp.
Product #7146 Made in the U.S.A.G7-1277
- PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label
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INGREDIENTS AND APPEARANCE
BEDSIDE-CARE
benzethonium chloride shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11701-053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 100 mg in 100 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) QUATERNIUM-15 (UNII: E40U03LEM0) GLYCERIN (UNII: PDC6A3C0OX) QUATERNIUM-52 (UNII: 588EQF3H1P) POLYSORBATE 20 (UNII: 7T1F30V5YH) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM LAUROAMPHOACETATE (UNII: SLK428451L) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11701-053-04 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/15/2009 2 NDC:11701-053-05 237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/15/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M003 06/15/2009 Labeler - Coloplast Corp (110326675) Registrant - Coloplast Corp. (847436391) Establishment Name Address ID/FEI Business Operations Medline Industries, LP 119451704 ANALYSIS(11701-053) , MANUFACTURE(11701-053)
