NDC | 72130-002-01, 72130-002-02 |
Set ID | eb1d4d76-c2df-475a-98bb-541a5ea75769 |
Category | HUMAN OTC DRUG LABEL |
Packager | Registered Chemicals Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SANISMART 2
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72130-002 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 WATER (UNII: 059QF0KO0R) COCO GLUCOSIDE (UNII: ICS790225B) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72130-002-02 1250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/01/2018 2 NDC:72130-002-01 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/01/2018 Labeler - Registered Chemicals Corporation (046652831)