Dosage and administration
●Apply to hands, allow to air dry without wiping. ●Children under 6 years of age should be supervised when using this product
Biopure antibacterial hand wipe fresh scent 75 ct
- Manufacturer
- Osike Cosmetics Co., Ltd.
- Effective date
- 2020-12-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:35:25
Label at a glance#
ProductWET WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections
Storage and handling
●Store in a cool, dry place, between 15°C-30°C（59°F-86°F） ●Avoid freezing and excessive heat above 40°C（104°F）
Label contents#
Full prescribing information#
Active Ingredient(s)
Benzalkonium Chloride 0.13% ……………………………………………...Antimicroblal
Purpose
Antimicroblal
Use
●Hand sanitizer to help reduce bacteria
●For use when soap and water are not available.
Warnings
For external use only.
Do not use
●in children less than 2 months old.
●on open skin wounds
OTC - WHEN USING SECTION
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
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
●Apply to hands, allow to air dry without wiping.
●Children under 6 years of age should be supervised when using this product
Other information
●Store in a cool, dry place, between 15°C-30°C（59°F-86°F）
●Avoid freezing and excessive heat above 40°C（104°F）
Inactive ingredients
Aloe Barbadensis Extract, Alpha-Tocopherol, Fragrance, Glycerin,
Phenoxyethanol, Propylene Glycol, Purified Water
Package Label - Principal Display Panel
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79866-010-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b3a-00bf-a426-e053-dadaa90af4c2 | 79866-010 WET WIPE |
| 79866-010-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b3a-00bf-a426-e053-dadaa90af4c2 | 79866-010 WET WIPE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79866-010-01 | WET WIPE | 40 in 1 DRUM | CLOTH | 40 | 3 | |
| 79866-010-02 | WET WIPE | 75 in 1 DRUM | CLOTH | 75 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- WET WIPE
- Wet wipes
- GLYCERIN
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- ALOE VERA LEAF
- WATER
- .ALPHA.-TOCOPHEROL, DL-
- PHENOXYETHANOL
- PROPYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79866-010 | 79866-010-01, 79866-010-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| .ALPHA.-TOCOPHEROL, DL- | 7QWA1RIO01 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | 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 |
|---|---|---|---|---|---|---|
| b6a38541-2884-59ca-e053-2a95a90a3844 | b5d744db-e80a-5e3a-e053-2995a90ac523 | 2020-12-17 | Warnings | b6a38541-2884-59ca-e053-2a95a90a3844 b5d744db-e80a-5e3a-e053-2995a90ac523 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.