Dosage and administration
■ Wet hands thoroughly with product and allow to dry without wiping ■ Do not flush
■ Wet hands thoroughly with product and allow to dry without wiping ■ Do not flush
Benzalkonium Chloride 0.1%
Water, Phenoxyethanol, Glycerin, Sodium benzoate, Polysorbate 20, Disodium EDTA, Tocopheryl acetate, Citric acid
Antiseptic
■ If swallowed, get medical help or contact a Posion Control Center right away
■ Instant hand antiseptic to decrease bacteria on the skin
Warnings
For external use only
Stop use and ask a doctor if
■ hypersensitivity symptoms such as erythema, itching and dermatitis happen
■ skin irritation happens
Do not use
■ in combination with soap or antibacterial cleansing agents
■ the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin
When using this product
■ avoid using repeatedly in the same area, skin irritation may occur
■ avoid getting into the eyes (if contact occurs, wash well with clean water)
■ if following abnormal symptoms persist, discontinue use: Irritation around the eyes, ears, mucous membranes, including the mouth, skin irritation, and rashes
■ Wet hands thoroughly with product and allow to dry without wiping
■ Do not flush
■ Read the directions and warnings before use ■ Avoid freezing and excessive heat above 40 ℃ (104 ℉)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73923-0130-1 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-9faa-d8a0-e053-dadaa90a6e4e | Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73923-0130-1 | Mediwiper | 850 g in 1 CONTAINER | LIQUID | 850 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 73923-0130 | MEDIWIPER (BENZALKONIUM CHLORIDE) LIQUID [FIRSTCHAM CO., LTD] | 1 | Legacy NDC, 1 package rows | 20201007_e6501e52-7c3f-41c8-ae61-3a38e43f4b18.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 73923-0130 | 73923-0130-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| Polysorbate 20 | 7T1F30V5YH | IACT |
| EDETATE DISODIUM ANHYDROUS | 8NLQ36F6MM | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | 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 |
|---|---|---|---|---|---|---|
| a8dbd01b-5f06-4b01-b295-01d6b4560de5 | e6501e52-7c3f-41c8-ae61-3a38e43f4b18 | 2020-10-06 | Warnings | a8dbd01b-5f06-4b01-b295-01d6b4560de5 e6501e52-7c3f-41c8-ae61-3a38e43f4b18 |
Adverse event summaries are temporarily unavailable. Other product information remains available.