Dosage and administration
Wet hands thoroughly with product and allow to dry.
Wet hands thoroughly with product and allow to dry.
Alcohol 62% w/w
Antiseptic
Decrease bacteria on hands.
For external use only.
Flammable.Keep product away from fire or flame.
When using this product
avoid contact with eyes; in case of contact, flush eyes with water.
Stop use and ask a doctor if
irritation or redness develops and persists.
If swallowed, get medical help or contact a Poison Control Center right away.
Wet hands thoroughly with product and allow to dry.
Water (Aqua), ACRYLATES/C10-30 ALKYL ACRYLATE CROSSCOPOLYMER, AMINOMETHYL PROPANOL, Fragrance (Parfum), Eucalyptus Citriodora Oil, Mentha Viridis (Spearmint) Leaf Oil, Argania Spinosa Kernel Oil, May Contain: D&C Red No. 33 (Cl17200), FD&C Red No.4 (Cl14700), FD&C Yellow No. 5 (Cl19140), FD&C Blue No. 1 (Cl 42090).
Warning - Choking Hazard
Small parts. Not for children under 3 years.
No Animal Testing
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 56136-413-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a4bd-d83d-e063-dadaa90ab31f | HAND SANITIZER |
| 56136-413-02 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a4bd-d83d-e063-dadaa90ab31f | HAND SANITIZER |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 56136-413-01 | Aromatherapy Hand Sanitizer eucalyptus and spearmint | 30 mL in 1 BOTTLE | GEL | 30 | 1 | |
| 56136-413-02 | Aromatherapy Hand Sanitizer eucalyptus and spearmint | 50 mL in 1 BOTTLE | GEL | 50 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 56136-413 | 56136-413-01, 56136-413-02 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CARBOMER COPOLYMER TYPE A | 71DD5V995L | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| SPEARMINT OIL | C3M81465G5 | IACT |
| ARGANIA SPINOSA LEAF | 51XV5WTF7E | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | CNTM |
| FD&C RED NO. 4 | X3W0AM1JLX | CNTM |
| FD&C YELLOW NO. 5 | I753WB2F1M | CNTM |
| FD&C BLUE NO. 1 | H3R47K3TBD | CNTM |
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 |
|---|---|---|---|---|---|---|
| 5e94c322-b0b3-47f2-99c0-617f7b3964b6 | c965bcff-c8fd-4709-8696-a0ccb30abf28 | 2020-10-17 | Warnings | 5e94c322-b0b3-47f2-99c0-617f7b3964b6 c965bcff-c8fd-4709-8696-a0ccb30abf28 |
Adverse event summaries are temporarily unavailable. Other product information remains available.