Indications and uses
Helps reduce bacteria that potentially can cause disease Helps prevent cross contamination by hand contact
Helps reduce bacteria that potentially can cause disease Helps prevent cross contamination by hand contact
Apply cleaner to palm of hand Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds Rinse with water until all cleaner is removed from hands Dry completely (incomplete drying may lead to chapped skin).
Drug Facts
Chloroxylenol (1.49% w/w)
Anti-Microbial Hand Cleanser
Water, 2-Propanol, Sodium Laureth Sulfate, Cocoamidopropyl Betaine, Cocoamphoproprionate,
Cocoamide, Hydroxyethyl Cellulose, Triclosan, FD&C Yellow #5, FD&C Red #40.
The container is coded for Recycling
510-003-100-501
Manufactured for:
Fikes Northwest, Corp.
13401 E. Trent Ave., Spokane Valley, WA 99216
(509) 926-0534 • (509) 755-0370 Fax
fikesnw@att.net •
www.fikesnorthwest.com
| Bottle Label: |
FIKES
Foaming Anti-Microbial
Food Service Hand Wash
An Anti-Microbial Lotion Hand Wash
Formulated To Clean Effectively,
Yet Gently. Reduces Total Cost Per Hand Wash
Keep Out Of Reach Of Children
CAUTION
See back panel for additional precautionary information.

| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50036-571-05 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-bda5-621f-e053-dbdaa90a74ad | FIKES Foaming Anti-Microbial Food Service Hand Wash |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50036-571-05 | FIKES Foaming Anti-Microbial Food Service Hand Wash | 3785 mL in 1 BOTTLE | LIQUID | 3785 | 1 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| chloroxylenol | ACTIVE INGREDIENT | 0F32U78V2Q | 1 | |
| chloroxylenol | ACTIVE MOIETY | 0F32U78V2Q | 1 | |
| cocamidopropyl betaine | INACTIVE INGREDIENT | 5OCF3O11KX | 1 | |
| coco diethanolamide | INACTIVE INGREDIENT | 92005F972D | 1 | |
| hydroxyethyl cellulose (2000 CPS at 1%) | INACTIVE INGREDIENT | S38J6RZN16 | 1 | |
| isopropyl alcohol | INACTIVE INGREDIENT | ND2M416302 | 1 | |
| sodium laureth sulfate | INACTIVE INGREDIENT | BPV390UAP0 | 1 | |
| triclosan | INACTIVE INGREDIENT | 4NM5039Y5X | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 50036-571 | 50036-571-05 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| chloroxylenol | 0F32U78V2Q | ACTIB |
| water | 059QF0KO0R | IACT |
| sodium laureth sulfate | BPV390UAP0 | IACT |
| cocamidopropyl betaine | 5OCF3O11KX | IACT |
| hydroxyethyl cellulose (2000 CPS at 1%) | S38J6RZN16 | IACT |
| isopropyl alcohol | ND2M416302 | IACT |
| coco diethanolamide | 92005F972D | IACT |
| triclosan | 4NM5039Y5X | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| coco diethanolamide | COCO DIETHANOLAMIDE | 92005F972D | SUSPENSION / TOPICAL | 4 %w/w | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SPRAY / NASAL | 0.1 mg/0.2ml | ||
| coco diethanolamide | COCO DIETHANOLAMIDE | 92005F972D | SPONGE / TOPICAL | 2 %w/w | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SOLUTION / TOPICAL | 0.21 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SUSPENSION / TOPICAL | 0.69 %w/v | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SOLUTION / TOPICAL | 40 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SUSPENSION / ORAL | 100 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | GEL / TOPICAL | 4 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SPONGE / TOPICAL | 4 %w/w | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| sodium laureth sulfate | SODIUM LAURETH-3 SULFATE | BPV390UAP0 | CAPSULE / ORAL | 3.5 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SUSPENSION / AURICULAR (OTIC) | 1 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | OIL / AURICULAR (OTIC) | 6 mg | ||
| coco diethanolamide | COCO DIETHANOLAMIDE | 92005F972D | SOLUTION / TOPICAL | 2.5 %w/v | ||
| sodium laureth sulfate | SODIUM LAURETH-3 SULFATE | BPV390UAP0 | CREAM / TOPICAL | NA | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | POWDER, FOR SUSPENSION / ORAL | 560 mg | ||
| coco diethanolamide | COCO DIETHANOLAMIDE | 92005F972D | CREAM / TOPICAL | 30 mg | ||
| coco diethanolamide | COCO DIETHANOLAMIDE | 92005F972D | SHAMPOO / TOPICAL | 600 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | OIL / TOPICAL | 72 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | TABLET, CHEWABLE / ORAL | 5.9 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | GEL, METERED / TOPICAL | 525 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SOLUTION/ DROPS / OPHTHALMIC | 0.5 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SUSPENSION / OPHTHALMIC | 0.25 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | LOTION / TOPICAL | 0.2 %w/v | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | TABLET, EXTENDED RELEASE / ORAL | 350 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SOLUTION / ORAL | 3 mg | ||
| sodium laureth sulfate | SODIUM LAURETH-3 SULFATE | BPV390UAP0 | TABLET / ORAL | 0.91 mg | ||
| sodium laureth sulfate | SODIUM LAURETH-3 SULFATE | BPV390UAP0 | SPRAY / TOPICAL | 0.1 %w/w | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | LOTION, AUGMENTED / TOPICAL | 2070 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SWAB / TOPICAL | 43.9 %w/w | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | GEL / TOPICAL | 75 mg | ||
| hydroxyethyl cellulose (2000 CPS at 1%) | HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) | S38J6RZN16 | SYRUP / ORAL | 2 mg/5ml | ||
| sodium laureth sulfate | SODIUM LAURETH-3 SULFATE | BPV390UAP0 | SHAMPOO / TOPICAL | 3192 mg |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 077f6779-3d56-4283-be25-8de99e7f4af0 | 9729472c-3000-4725-8520-32eb5e711592 | 2010-09-03 | Warnings | 077f6779-3d56-4283-be25-8de99e7f4af0 9729472c-3000-4725-8520-32eb5e711592 |
Adverse event summaries are temporarily unavailable. Other product information remains available.