Indications and uses
for hand sanitizing to decrease bacteria on the skin recommended for repeated use
for hand sanitizing to decrease bacteria on the skin recommended for repeated use
take wipe and rub thoroughly over all surfaces ofboth hands ·rub hands together briskly to dry·dispose of wipe
benzalkonium chloride 0.13%
Antibacterial
for hand sanitizing to decrease bacteria on the skin
recommended for repeated use
For External use only.
Do not use if you are allergic to any of the ingredients.
When using this product avoid contact with the eyes,in case of contact, flush eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness develop .
keep out of reach of children .if swallowed, get medical help or contact a Poison Control Center right away.
take wipe and rub thoroughly over all surfaces ofboth hands
·rub hands together briskly to dry·dispose of wipe
WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1038558 | benzalkonium chloride 0.13 % Medicated Pad | PSN | 2 |
| 1038558 | benzalkonium chloride 1.3 MG/ML Medicated Pad | SCD | 2 |
| 1038558 | benzalkonium chloride 0.13 % Topical Cloth | SY | 2 |
| 1038558 | benzalkonium chloride 0.13 % Topical Swab | SY | 2 |
| 1038558 | benzalkonium chloride 0.13 GM per 100 GM Topical Pad | SY | 2 |
| 1038558 | benzalkonium chloride 0.13 GM per 100 GM Topical Swab | SY | 2 |
| 1038558 | benzalkonium chloride 1 ML per 750 ML Topical Swab | SY | 2 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73326-002-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-aa2d-a426-e053-dadaa90af4c2 | Antibacterial Wet Wipes |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73326-002-01 | Antibacterial Wet Wipes | 48 in 1 CARTON | SWAB | 48 | 2 | |
| 73326-002-01 | Antibacterial Wet Wipes | 30 in 1 BAG | SWAB | 30 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 73326-002 | 73326-002-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| GOSSYPIUM BARBADENSE LEAF | 251DUP3OSN | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| METHYLISOTHIAZOLINONE | 229D0E1QFA | IACT |
| METHYLCHLOROISOTHIAZOLINONE | DEL7T5QRPN | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| a921ef64-8143-b2a3-e053-2995a90a56bd | 9270204a-c913-00a8-e053-2995a90a10f7 | 2020-06-28 | Warnings | a921ef64-8143-b2a3-e053-2995a90a56bd 9270204a-c913-00a8-e053-2995a90a10f7 |
Adverse event summaries are temporarily unavailable. Other product information remains available.