Disinfecting Wipes
Wipes containing the active ingredient are used topically and externally.
Wipes containing the active ingredient are used topically and externally.
Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Stop use and ask a doctor if irritation and redness develop or such condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
INACTIVE INGREDIENTS:
Aloe Barbadensis Leaf, Fragrance, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Tocopheryl Acetate, Water
To decrease bacteria on skin that could cause disease. For external use only.
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away. For children under 6, use only under adult supervision. Not recommended for infants.
To decrease bacteria on skin that could cause disease.
ACTIVE INGREDIENTS:
Benzalkonium Chloride 0.13%
1L NDC: 81344-002-01
| 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 |
|---|---|---|---|---|---|
| 81344-002-01 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a3a3-d8a0-e053-dadaa90a6e4e | Disinfecting Wipes |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81344-002-01 | Disinfecting Wipes | 80 in 1 CONTAINER | CLOTH | 80 | 1 | |
| 81344-002-01 | Disinfecting Wipes | 1300 mL in 1 CONTAINER | CLOTH | 1300 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 81344-002 | 81344-002-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| b7a7b91a-cbeb-71c2-e053-2995a90a30ec | b7a7b91a-cbea-71c2-e053-2995a90a30ec | 2021-01-12 | Warnings | b7a7b91a-cbeb-71c2-e053-2995a90a30ec b7a7b91a-cbea-71c2-e053-2995a90a30ec |
Adverse event summaries are temporarily unavailable. Other product information remains available.