Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping.
Wet hands thoroughly with product and allow to dry without wiping.
Store at 68 to 77F (20-25C) Do not store above 110F (43C) You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536
Alcohol Denat. 62%
Antiseptic
Use for hand-washing to decrease bacteria on the skin, only when water it not available.
For external use only. Flammable, keep away from fire and flames.
Do not get into eyes.
If contact occurs, rinse eyes thoroughly with water.
If irritation and redness develop.
If swallowed, get medical help or contact a Poison Control Center right away.
Wet hands thoroughly with product and allow to dry without wiping.
Store at 68 to 77F (20-25C)
Do not store above 110F (43C)
You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536
Water,
Glycerin,
Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Fragrance,
Aloe Barbadensis Leaf Extract,
Polysorbate 20,
Sodium Hydroxide,
Red 33,
Blue 1
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51522-055-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-93a0-a426-e053-dadaa90af4c2 | Ultra Defense Sani Smart Vanilla Lavender Hand Sanitizer |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51522-055-01 | Ultra Defense Sani Smart Vanilla Lavender Hand Sanitizer | 236 mL in 1 BOTTLE, PLASTIC | GEL | 236 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 51522-055 | 51522-055-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) | 59TL3WG5CO | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
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 |
|---|---|---|---|---|---|---|
| ac2decf1-0f4d-20b3-e053-2995a90a4eb5 | ac2decf1-0f4c-20b3-e053-2995a90a4eb5 | 2020-08-06 | Warnings | ac2decf1-0f4d-20b3-e053-2995a90a4eb5 ac2decf1-0f4c-20b3-e053-2995a90a4eb5 |
Adverse event summaries are temporarily unavailable. Other product information remains available.