Label: QUALITY CHOICE MERTHIOLATE- benzalkonium chloride liquid
- NDC Code(s): 63868-493-02
- Packager: Chain Drug Market Association
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 20, 2023
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE MERTHIOLATE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-493 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) ALCOHOL (UNII: 3K9958V90M) ACETONE (UNII: 1364PS73AF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-493-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/12/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 03/25/1998 Labeler - Chain Drug Market Association (011920774) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 analysis(63868-493) , manufacture(63868-493) , pack(63868-493) , label(63868-493)