NDC | 21749-090-22, 21749-090-42, 21749-090-67 |
Set ID | 916cf0e6-da14-4f09-8d99-bea694609bea |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PROVON FOAMING ANTIMICROBIAL HANDWASH WITH MOISTURIZERS
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-090 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) LACTIC ACID (UNII: 33X04XA5AT) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) JOJOBA OIL (UNII: 724GKU717M) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) CORN OIL (UNII: 8470G57WFM) AMMONIUM SULFATE (UNII: SU46BAM238) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-090-22 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2003 2 NDC:21749-090-42 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2003 3 NDC:21749-090-67 2000 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/13/2003 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/13/2003 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 MANUFACTURE(21749-090) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 label(21749-090) , pack(21749-090)