NDC | 71925-400-40, 71925-400-42 |
Set ID | 5e913d83-1d63-4065-a820-7a3e5aa22ecf |
Category | HUMAN OTC DRUG LABEL |
Packager | Pollock Investments Incorporated |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RADIANCE ANTIBACTERIAL PLUM FOAM HANDWASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71925-400 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.005 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Glycerin (UNII: PDC6A3C0OX) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) PEG-80 Sorbitan Laurate (UNII: 239B50Y732) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Ethylhexylglycerin (UNII: 147D247K3P) Lauramine Oxide (UNII: 4F6FC4MI8W) POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH) PHENOXYETHANOL (UNII: HIE492ZZ3T) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71925-400-40 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/30/2017 2 NDC:71925-400-42 1250 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/30/2017 Labeler - Pollock Investments Incorporated (007366958)