Dosage and administration
Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.
Multi-purpose Antibacterial Wet Wipes
- Manufacturer
- NUVOMED,INC.
- Effective date
- 2023-11-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:20:18
Label at a glance#
ProductMulti-purpose Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections
Storage and handling
The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active Ingredient(s)
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial Agent
Use
Decreases bacteria on skin.
Warnings
For external use only.
Do not use
Do not use if you are allergic to any of the ingredients.
OTC - WHEN USING SECTION
Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.
Other information
The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.
Inactive ingredients
C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.
Package Label - Principal Display Panel
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Multi-purpose Antibacterial Wet Wipes
- BENZALKONIUM CHLORIDE
- N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)
- DECYL GLUCOSIDE
- WATER
- BENZALKONIUM
- PROPYLENE GLYCOL
- EDETATE DISODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78927-003 | 78927-003-01, 78927-003-02, 78927-003-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) | G258TFN61X | IACT |
| DECYL GLUCOSIDE | Z17H97EA6Y | IACT |
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | 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 |
|---|---|---|---|---|---|---|
| 4726cac9-139d-c4ed-e063-6294a90a2a98 | a7eba769-a99f-66b6-e053-2995a90ab85a | 2025-12-30 | Warnings | a7eba769-a99f-66b6-e053-2995a90ab85a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.