Label: MERTHIOLATE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 0395-9122-92 - Packager: Humco Holding Group, 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 June 20, 2020
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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 aska doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- Quality Choice Label
- Premier Value
- DDM
- CVS Label
- Vida Mia Label
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INGREDIENTS AND APPEARANCE
MERTHIOLATE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0395-9122 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:0395-9122-92 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/14/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/25/1998 Labeler - Humco Holding Group, Inc. (825672884) Registrant - Humco Holding Group, Inc. (825672884) Establishment Name Address ID/FEI Business Operations Humco Holding Group, Inc. 825672884 manufacture(0395-9122) , analysis(0395-9122) , pack(0395-9122) , label(0395-9122)