Label: MEDPRIDE ANTIBACTERIAL HAND WASH- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 52410-8091-1 - Packager: Shield Line LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 13, 2022
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- Drug Facts
- Active Ingredient
- Purpose
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- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDPRIDE ANTIBACTERIAL HAND WASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52410-8091 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength LIMONENE, (+)- (UNII: GFD7C86Q1W) COCO DIETHANOLAMIDE (UNII: 92005F972D) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SULISOBENZONE (UNII: 1W6L629B4K) SODIUM CHLORIDE (UNII: 451W47IQ8X) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) GLYCERIN (UNII: PDC6A3C0OX) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52410-8091-1 400 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/04/2020 Labeler - Shield Line LLC (078518916)