Label: MERINGUE FOAMING ANTIBACTERIAL HAND- benzalkonium chloride solution
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Contains inactivated NDC Code(s)
NDC Code(s): 63998-010-27 - Packager: United Laboratories, Inc.
- 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 11, 2018
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- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
UNITED LABORATORIES
United 758
MERINGUE
Foaming Antibacterial Hand Soap
PRECAUCION AL USARIO: Si usted no pede leer Ingles, pregunte a alguien que le traduzca esta etigueta para usted antes de uso.
A high-quality, foam soap that is 99.99% effective against common bacteria.
An SDS for this product is available through United’s website, www.unitedlabsinc.com, providing 24 hour access. Please read the SDS carefully and follow all directions when using or handling this product. Never reuse empty containers. Incompatible materials may adversely react.
NDC 63998-010-27
Manufactured in U.S.A.
1017
1 L (33.8 fl oz)Sold By: UNITED LABORATORIES, INC.
320 37th Avenue ● St. Charles, IL 60174 ● 1-800-323-2594 ● www.unitedlabsinc.com
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INGREDIENTS AND APPEARANCE
MERINGUE FOAMING ANTIBACTERIAL HAND
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63998-010 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LACTIC ACID (UNII: 33X04XA5AT) SALICYLIC ACID (UNII: O414PZ4LPZ) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63998-010-27 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/11/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/11/2018 Labeler - United Laboratories, Inc. (001759737)