Active Ingredient
Active ingredient for this sanitizing alcohol-free wipes is Benzalkonium chloride
.
Active ingredient for this sanitizing alcohol-free wipes is Benzalkonium chloride
.
Hand Sanitizer to help decrease bacteria on the skin.
For dispensing: Peel back front label at tab. Remove towelette wipes as needed. Reseal pouch by pressing label firmly back into place.
For use: Apply thoroughly to hands as desired. Allow to dry without wiping. Discard wipe in trash after use. Do not flush.
For external use only.
Do not use in or near the eyes. If contact occurs, flush thoroughly with water.
Stop use and contact doctor if redness and irritation develops and persists.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Aqua (Water), Polyaminopropyl Biguanide, Xylitol Extract, Aloe Barbadensis Leaf Extract.
FOR DISPENSING: Peel back front label at tab. Remove towelette wipes as needed.
FOR USE: Apply thoroughly to hands asdesired. Allow to dry without wiping.
20-pack. NDC: 80380-100-01
.
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1038558 | benzalkonium chloride 0.13 % Medicated Pad | PSN | 1 |
| 1038558 | benzalkonium chloride 1.3 MG/ML Medicated Pad | SCD | 1 |
| 1038558 | benzalkonium chloride 0.13 % Topical Cloth | SY | 1 |
| 1038558 | benzalkonium chloride 0.13 % Topical Swab | SY | 1 |
| 1038558 | benzalkonium chloride 0.13 GM per 100 GM Topical Pad | SY | 1 |
| 1038558 | benzalkonium chloride 0.13 GM per 100 GM Topical Swab | SY | 1 |
| 1038558 | benzalkonium chloride 1 ML per 750 ML Topical Swab | SY | 1 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 80380-100-01 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-204f-fd44-e053-dadaa90aa01b | b1c1c819-e35a-6c60-e053-2a95a90aa104 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80380-100-01 | Sanitizing Alcohol Free Wipes | 20 mg in 1 PACKET | CLOTH | 20 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 80380-100 | 80380-100-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POLYAMINOPROPYL BIGUANIDE | DT9D8Z79ET | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| XYLITOL | VCQ006KQ1E | IACT |
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 |
|---|---|---|---|---|---|---|
| b1c1c819-e34c-6c60-e053-2a95a90aa104 | b1c1c819-e35a-6c60-e053-2a95a90aa104 | 2020-10-23 | Warnings | b1c1c819-e34c-6c60-e053-2a95a90aa104 b1c1c819-e35a-6c60-e053-2a95a90aa104 |
Adverse event summaries are temporarily unavailable. Other product information remains available.