Antibacterial Hand Wipes
- Manufacturer
- Karza Med Group, LLC | NINGBO RIWAY NONWOVENS TECH CO., LTD9
- Effective date
- 2020-05-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:21:19
Label at a glance#
Label contents#
Full prescribing information#
DOSAGE & ADMINISTRATION SECTION
Add Water to Moisten Cloth. Rub Cloth to build Later. Air or Towel Dry
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Cocmedyl Propyl Betain, Sodium Lauryl Ether Sulfate, Postassion Sorbate, Sodium Chloride, 1,2 Propendiol, Citric Acid, Sodium Myristate, Sodium Dodcyl Sulfate, Fatty Esther Ethioxylates, Vitamin E, Aloe Vera.
INDICATIONS & USAGE SECTION
For Hand Sanitizing and Decreasing Bacteria on Hands. If irritation occurs stop usage.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of Reach of Children.
OTC - PURPOSE SECTION
Purpose: Antibacterial
WARNINGS SECTION
Warning, For external use Only
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76749-020-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-5739-a426-e053-dadaa90af4c2 | Anti Bacterial Soap |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76749-020-02 | Antibacterial Hand Wipes | 24 g in 1 BAG | CLOTH | 24 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Antibacterial Hand Wipes
- Benzalkonium Chloride
- POTASSIUM SORBATE
- SODIUM LAURYL SULFATE
- .ALPHA.-TOCOPHEROL
- BENZALKONIUM
- WATER
- SODIUM BENZOATE
- SODIUM MYRISTATE
- PROPYLENE GLYCOL
- COCAMIDOPROPYL BETAINE
- SODIUM LAURATE
- SODIUM LAURETH SULFATE
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76749-020 | 76749-020-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| .ALPHA.-TOCOPHEROL | H4N855PNZ1 | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SODIUM MYRISTATE | 06BLC4V0IV | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| SODIUM LAURATE | K146MR5EXO | IACT |
| SODIUM LAURETH SULFATE | BPV390UAP0 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| a49a6a82-f28d-e2e2-e053-2a95a90a564c | a49a6a82-f28c-e2e2-e053-2a95a90a564c | 2020-05-01 | Warnings | a49a6a82-f28d-e2e2-e053-2a95a90a564c a49a6a82-f28c-e2e2-e053-2a95a90a564c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


