Label: MG DERMASAN- n/a liquid
- NDC Code(s): 50241-259-01, 50241-259-02
- Packager: Morgan Gallacher Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 14, 2023
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- Active Ingredient
- Uses
- Purpose
- Warnings
- Keep out of reach of children
- Directions
- Inert Ingredients
- MG DermaSan
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INGREDIENTS AND APPEARANCE
MG DERMASAN
n/a liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50241-259 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) GLYCERETH-17 COCOATE (UNII: 3057VPT0KC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50241-259-02 1 in 1 BOX 10/01/2018 1 NDC:50241-259-01 3756 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2018 Labeler - Morgan Gallacher Inc. (028311595) Registrant - Morgan Gallacher Inc. (028311595) Establishment Name Address ID/FEI Business Operations Morgan Gallacher Inc. 028311595 manufacture(50241-259) , api manufacture(50241-259) , pack(50241-259)