Dosage and administration
Apply to hands and skin. No rinsing required. Discard after use. Children under 6 years of age should be supervised when using this product.
Apply to hands and skin. No rinsing required. Discard after use. Children under 6 years of age should be supervised when using this product.
Avoid freezing and store below 110F (43C). Dispose the used wipe in trash, do not flush it into the toilet. May discolor certain fabrics or surfaces.
Alcohol 75% v/v. Purpose: Antiseptic
Antiseptic
For sanitizing and to help reduce bacteria on the skin. For use when soap and water are not available.
For external use only. Flammable. Keep away from heat or flame
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Apply to hands and skin. No rinsing required. Discard after use.
Children under 6 years of age should be supervised when using this product.
Avoid freezing and store below 110F (43C).
Dispose the used wipe in trash, do not flush it into the toilet.
May discolor certain fabrics or surfaces.
2 phenaxythanol, benzalkonium chloride, didecyl dimethyl ammonium, ethylhexylglycerin, propylene glycol, water
50 PCS NDC: 79040-122-01
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79040-122-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-9722-a426-e053-dadaa90af4c2 | Pharma Cleanse Wipe 50 PCS TEST |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79040-122-01 | Pharma Health | 50 in 1 BAG | CLOTH | 50 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 79040-122 | 79040-122-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| DIDECYLDIMONIUM CHLORIDE | JXN40O9Y9B | 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 |
|---|---|---|---|---|---|---|
| b1440228-e2c4-921c-e053-2a95a90a65f0 | b1440228-e2c5-921c-e053-2a95a90a65f0 | 2020-10-02 | Warnings | b1440228-e2c4-921c-e053-2a95a90a65f0 b1440228-e2c5-921c-e053-2a95a90a65f0 |
Adverse event summaries are temporarily unavailable. Other product information remains available.