Dosage and administration
Wipe the skin and let it dry naturally. Supervise children under 6 years of age when using this product to avoid swallowing.
BABY WIPE PREMIUM
- Manufacturer
- SHINWA INTERNATIONAL CORPORATION
- Effective date
- 2021-05-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:40:21
Label at a glance#
ProductBABY WIPE PREMIUM
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections
Storage and handling
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
BABY WIPE PREMIUM
Active Ingredient(s)
BENZALKONIUM CHLORIDE 0.1% w/w, Antiseptic
Purpose
Antiseptic, BABY WIPE PREMIUM
Use
BABY WIPE PREMIUM to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
Do not use
- on open skin wounds
OTC - WHEN USING SECTION
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.
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
- Wipe the skin and let it dry naturally.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients
PURIFIED WATER
PROPYLEN GLYCOL
DISODIUM COCOAMPHODIACETATE
2-BROMO-2-NITROPROPANE 1.3-DIOL
Package Label - Principal Display Panel
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81889-501-01 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a6db-d8a0-e053-dadaa90a6e4e | BABY WIPE PREMIUM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81889-501-01 | BABY WIPE PREMIUM | 50 in 1 BAG | CLOTH | 50 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- BABY WIPE PREMIUM
- HIGH QUALITY COTTON NON-WOVEN FABRIC
- DISODIUM COCOAMPHODIACETATE
- BRONOPOL
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- PROPYLENE GLYCOL
- WATER
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81889-501 | 81889-501-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DISODIUM COCOAMPHODIACETATE | 18L9G3U51M | IACT |
| BRONOPOL | 6PU1E16C9W | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | 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 |
|---|---|---|---|---|---|---|
| c23138c0-f7ee-f3c1-e053-2a95a90ab535 | c2313202-0e5c-5c85-e053-2a95a90ace47 | 2021-05-13 | Warnings | c23138c0-f7ee-f3c1-e053-2a95a90ab535 c2313202-0e5c-5c85-e053-2a95a90ace47 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.