NDC | 30805-010-02, 30805-010-05, 30805-010-07, 30805-010-09 |
Set ID | 2750f62c-e650-428a-b070-5c13ff8e378e |
Category | HUMAN OTC DRUG LABEL |
Packager | Buckeye International, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30805-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.12 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) EDETATE SODIUM (UNII: MP1J8420LU) Allantoin (UNII: 344S277G0Z) Aloe Vera Leaf (UNII: ZY81Z83H0X) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) Methylisothiazolinone (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30805-010-02 1250 mL in 1 BAG; Type 0: Not a Combination Product 11/01/2011 2 NDC:30805-010-05 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2011 3 NDC:30805-010-07 550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2011 4 NDC:30805-010-09 1000 mL in 1 BAG; Type 0: Not a Combination Product 04/07/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/01/2011 Labeler - Buckeye International, Inc. (077132280) Establishment Name Address ID/FEI Business Operations Buckeye International, Inc. 077132280 manufacture(30805-010)