NDC | 21749-533-89, 21749-533-90, 21749-533-97 |
Set ID | db57037d-8827-4438-9729-1c2c49db529c |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PROVON ANTIBACTERIAL FOAM HANDWASH
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-533 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) LAURIC ACID (UNII: 1160N9NU9U) MONOETHANOLAMINE (UNII: 5KV86114PT) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) LACTIC ACID (UNII: 33X04XA5AT) ISOPROPYL ALCOHOL (UNII: ND2M416302) POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J) POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS) SODIUM METABISULFITE (UNII: 4VON5FNS3C) SODIUM SULFITE (UNII: VTK01UQK3G) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM SULFATE (UNII: 0YPR65R21J) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-533-89 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2013 2 NDC:21749-533-90 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2013 3 NDC:21749-533-97 700 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2013 12/01/2021 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-533)