Label: DIAL ANTIMICROBIAL- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57702-500-08 - 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 January 11, 2021
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Aqua (Water, Eau), Lauramidopropylamine Oxide, Glycerin, Lauramine Oxide, Cetrimonium Chloride, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Citric Acid, Sodium Benzoate, Myristamidopropylamine Oxide, Parfum (Fragrance), Zinc Sulfate, Dimethyl Lauramine, Tetrasodium EDTA, Alcohol, Camellia Sinensis Leaf Extract, Dimethyl Myristamine, CI 42090 (Blue 1), CI 17200 (Red 33)
- QUESTIONS
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAL ANTIMICROBIAL
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-500 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) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) GLYCERIN (UNII: PDC6A3C0OX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2) SODIUM BENZOATE (UNII: OJ245FE5EU) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) ALCOHOL (UNII: 3K9958V90M) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) CHAMOMILE (UNII: FGL3685T2X) ZINC SULFATE (UNII: 89DS0H96TB) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57702-500-08 221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/17/2020 Labeler - Bocchi Laboratories (013579387) Registrant - Henkel Corporation (081264055) Establishment Name Address ID/FEI Business Operations Bocchi Laboratories 013579387 manufacture(57702-500)