Label: DIAL ANTIMICROBIAL- benzalkonium chloride liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 57702-501-08 - Packager: Bocchi Laboratories
- 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 May 11, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- WHEN USING
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DIAL ANTIMICROBIAL
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 g in 100 mL Inactive Ingredients Ingredient Name Strength DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2) SODIUM BENZOATE (UNII: OJ245FE5EU) ALCOHOL (UNII: 3K9958V90M) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) ZINC SULFATE (UNII: 89DS0H96TB) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57702-501-08 221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/07/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/07/2021 Labeler - Bocchi Laboratories (013579387) Registrant - Henkel Corporation (081264055) Establishment Name Address ID/FEI Business Operations Bocchi Laboratories 013579387 manufacture(57702-501)