Indications and uses
1.Hand sanitizer to help reducebacteria on the skin. 2.For use when soap and water are not available.
Wet Wipes
- Manufacturer
- Shandong Tricol Marine Biological Technology Co.,Ltd
- Effective date
- 2020-11-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:33:50
Label at a glance#
ProductWet Wipes
Active ingredientBENZETHONIUM CHLORIDE
Label structure12 sections
Dosage and administration
1.open resealable label and pull one sheet from pack. 2.Thoroughly clean hands or affected area and discard in receptacle.Do not flush. 3.Allow to dry without wiping. 4.Be sure to reseal label completely to retain moisture.
Label contents#
Full prescribing information#
Uses
1.Hand sanitizer to help reducebacteria on the skin.
2.For use when soap and water are not available.
WARNINGS SECTION
For external use only. Flammable.Keep away from heat or flame.
OTC - DO NOT USE SECTION
Do not use on open skin wounds.
Do not use in children less than 2months of age.
OTC - WHEN USING SECTION
When using this product, keep out of reach of eyes and mouth. In case of contact with eyes,rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor irritation or rash occours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. lf swallowed,get medical help,or contact a Poison Control Center right away.
Directions
1.open resealable label and pull one sheet from pack.
2.Thoroughly clean hands or affected area and discard in receptacle.Do not flush.
3.Allow to dry without wiping.
4.Be sure to reseal label completely to retain moisture.
Other Information
Store at room temperature.
INACTIVE INGREDIENT SECTION
Water,Benzethonium chloride,Cetylpyridinium chloride anhydrous, Chlorphenesin,Propylene glycol,Phenoxyethanol,Ethylhexylglycerin, Pyrithione Sodium
OTC - ACTIVE INGREDIENT SECTION
Benzethonium chloride
OTC - PURPOSE SECTION
Antiseptic
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54156-001-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-b37b-a426-e053-dadaa90af4c2 | b359c5cd-631c-5b8a-e053-2a95a90a32f6 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54156-001-01 | Wet Wipes | 0.03 g in 1 PATCH | CLOTH | 0.03 | 1 | |
| 54156-001-01 | Wet Wipes | 20 in 1 PACKET | CLOTH | 20 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Wet Wipes
- WATER
- PYRITHIONE SODIUM
- CHLORPHENESIN
- BENZETHONIUM CHLORIDE
- BENZETHONIUM
- CETYLPYRIDINIUM CHLORIDE ANHYDROUS
- PHENOXYETHANOL
- PROPYLENE GLYCOL
- ETHYLHEXYLGLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 54156-001 | 54156-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| PYRITHIONE SODIUM | 6L3991491R | IACT |
| CHLORPHENESIN | I670DAL4SZ | IACT |
| BENZETHONIUM CHLORIDE | PH41D05744 | ACTIB |
| CETYLPYRIDINIUM CHLORIDE ANHYDROUS | 6BR7T22E2S | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ETHYLHEXYLGLYCERIN | 147D247K3P | IACT |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| b359c5cd-631d-5b8a-e053-2a95a90a32f6 | b359c5cd-631c-5b8a-e053-2a95a90a32f6 | 2020-11-05 | Warnings | b359c5cd-631d-5b8a-e053-2a95a90a32f6 b359c5cd-631c-5b8a-e053-2a95a90a32f6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.