Label: MAINTENANCE WAREHOUSE- benzalkonium chloride soap
- NDC Code(s): 18949-710-04
- Packager: HD Supply Facilities Maintenance, Ltd
- 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 April 18, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Antibacterial Hand Soap Active Ingredient
- Antibacterial Hand Soap
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Antibacterial Hand Soap
Warnings
- For external use only.
- Avoid contact with eyes.
- Children under the age of 6 should be supervised by an adult when using this product.
- Discontinue use is irritation or redness develops.
- If irritation persists for more than 72 hours, consult a physician.
- KEEP OUT OF REACH OF CHILDREN.
- If swallowed, get medical help or contact a Posion Control Center right away.
- Antibacterial Hand Soap
-
Antibacterial Hand Soap
Inactive Ingredients
Water, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Propylene Glycol, Sodium Chloride, Glycerin, PEG-4 Rapeseedamide, Dimethicone PEG-7 Cocoate, Ethanol, Fragrance, Bronopol, Diisoporpanolamine, Magnesium Nitrate, FD&C Yellow #5, Methychloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, FD&C Red #40.
- Antibacterial Hand Soap
- Antibacterial Hand Soap
- Antibacterial Hand Soap
- Antibacterial Hand Soap
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INGREDIENTS AND APPEARANCE
MAINTENANCE WAREHOUSE
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:18949-710 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLYCERIN (UNII: PDC6A3C0OX) PEG-4 RAPESEEDAMIDE (UNII: 89575CN928) DIMETHICONE (UNII: 92RU3N3Y1O) COCONUT ACID (UNII: 40U37V505D) ALCOHOL (UNII: 3K9958V90M) BRONOPOL (UNII: 6PU1E16C9W) DIISOPROPANOLAMINE (UNII: 0W44HYL8T5) MAGNESIUM NITRATE (UNII: 77CBG3UN78) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:18949-710-04 3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/15/2019 Labeler - HD Supply Facilities Maintenance, Ltd (171218949) Registrant - Betco Corporation, Ltd. (024492831) Establishment Name Address ID/FEI Business Operations Betco Corporation, Ltd. 024492831 manufacture(18949-710) , label(18949-710) , pack(18949-710)
