Label: PREMIER VALUE MERTHIOALATE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 68016-437-00 - Packager: Chain Drug Consortium
- Category: HUMAN OTC DRUG LABEL
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 December 13, 2017
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- Official Label (Printer Friendly)
- Premier Value Merthiolate
- Active Ingredient
- Purpose
- Indications
- Warnings
- Ask a doctor before use if you have
- When using this product do not
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Inactive Ingredient
- Label
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INGREDIENTS AND APPEARANCE
PREMIER VALUE MERTHIOALATE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-437 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 ACETONE (UNII: 1364PS73AF) FD&C RED NO. 4 (UNII: X3W0AM1JLX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-437-00 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/26/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/26/2017 Labeler - Chain Drug Consortium (101668460) Registrant - Humco Holding Group, Inc. (825672884) Establishment Name Address ID/FEI Business Operations Humco Holding Group, Inc. 825672884 manufacture(68016-437) , analysis(68016-437) , pack(68016-437) , label(68016-437)