NDC | 60193-202-01, 60193-202-03, 60193-202-05, 60193-202-07 |
Set ID | 52f9554b-e760-411b-9911-93b8915ff55e |
Category | HUMAN OTC DRUG LABEL |
Packager | Pacific World Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
WOODWARDS HANDCLENS FOAMING SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60193-202 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 WATER (UNII: 059QF0KO0R) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) ALLANTOIN (UNII: 344S277G0Z) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60193-202-01 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:60193-202-03 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 3 NDC:60193-202-05 1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 4 NDC:60193-202-07 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333A 05/01/2014 Labeler - Pacific World Corporation (089693097)