- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WOUND WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50332-0043 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .0013 g in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50332-0043-2 20 in 1 BOX 04/01/1974 1 1.4 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:50332-0043-0 10 in 1 BOX 04/01/1974 2 1.4 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:50332-0043-5 5 in 1 BOX 04/01/1974 3 1.4 g in 1 PACKET; Type 0: Not a Combination Product 4 NDC:50332-0043-7 100 in 1 BOX 04/20/2016 4 1.4 g in 1 PACKET; 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 01/01/1974 Labeler - HART Health (069560969)