Indications and uses
Uses ■ Hand sanitizer to decrease bacteria on the skin that could cause disease
I.D Hand Sanitizer
- Manufacturer
- THE SUN CO.LTD
- Effective date
- 2020-04-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:06:15
Label at a glance#
ProductI.D Hand Sanitizer
Active ingredientAlcohol
Label structure10 sections
Dosage and administration
Directions ■ Take an appropriate amount on your hands and rub thoroughly to dry. ■ For children under 6, use only under adult supervision ■ not recommended for infants
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active ingredients: Ethyl alcohol 70.0 %v/v
INACTIVE INGREDIENT
Inactive ingredients:
Water, Glycerin, Aloe Vera Gel, Grapefruit Seed Extract , Green Extract
PURPOSE
PURPOSE: Antiseptic
WARNINGS
Warnings:
For external use only-hands
Flammable. Keep away from heat and flame.
When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.
Stop use and ask a doctor if skin irritation or rash develops.
KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Uses
Uses
■ Hand sanitizer to decrease bacteria on the skin that could cause disease
Directions
Directions
■ Take an appropriate amount on your hands and rub thoroughly to dry.
■ For children under 6, use only under adult supervision
■ not recommended for infants
Other Information
Other Information
■ Read the directions and warnings before use
■ Avoid freezing and excessive heat above 40 degree C (104 degree F)
■ Storing the product in a different container may cause accidents or
deterioration of quality. Therefore, keep the product in its original container.
■ May discolor some fabrics or surfaces.
QUESTIONS
Questions
www thesunin.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74923-060-01 | 2023-01-30 | C162847 | 48780-1 | f386c64a-2e77-0266-e053-dadaa90a7c1a | e156b157-ceb0-41f7-a8fe-ad9c940db57d |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74923-060-01 | I.D Hand Sanitizer | 100 mL in 1 CONTAINER | GEL | 100 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- I.D Hand Sanitizer
- Alcohol
- Water
- GLYCERIN
- ALOE VERA LEAF
- CITRUS PARADISI SEED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74923-060 | 74923-060-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Alcohol | 3K9958V90M | ACTIB |
| Water | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| CITRUS PARADISI SEED | 12F08874Y7 | 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 |
|---|---|---|---|---|---|---|
| 59fa1c36-b0d9-422e-9bc4-f9f48b01c7cd | e156b157-ceb0-41f7-a8fe-ad9c940db57d | 2020-04-14 | Warnings | 59fa1c36-b0d9-422e-9bc4-f9f48b01c7cd e156b157-ceb0-41f7-a8fe-ad9c940db57d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.