Dosage and administration
Wet hands thoroughly with product and allow to dry.
Wet hands thoroughly with product and allow to dry.
Alcohol 65%
Antiseptic
Decrease bacteria on hands
For external use only.
avoid contact with eyes; in case of contact, flush eyes with water.
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/c 10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrace (Parfum). May contain: FD&C No. 4 (C.l. 14700), D&C Red No. 33 (Cl 17200), FD&C Yellow 5, FD&C Blue No. 1 (Cl 42090).
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 56136-089-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-aeed-d83d-e063-dadaa90ab31f | hand sanitizer |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 56136-089-01 | Follow the Rainbow Antibacterial Hand Sanitizer Watermelon Ice Pop scented | 236 mL in 1 BOTTLE | GEL | 236 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 56136-089 | FOLLOW THE RAINBOW ANTIBACTERIAL HAND SANITIZER WATERMELON ICE POP SCENTED (ALCOHOL) GEL [GANZHOU OLIVEE COSMETIC CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200730_36de61f3-613e-4420-a531-2e00d2b89811.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 56136-089 | 56136-089-01 |
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 |
| GLYCERIN | PDC6A3C0OX | IACT |
| FD&C RED NO. 4 | X3W0AM1JLX | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | 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 |
|---|---|---|---|---|---|---|
| fa430bf6-41d1-4603-a5cf-6b8ad412de59 | 36de61f3-613e-4420-a531-2e00d2b89811 | 2020-07-30 | Warnings | fa430bf6-41d1-4603-a5cf-6b8ad412de59 36de61f3-613e-4420-a531-2e00d2b89811 |
Adverse event summaries are temporarily unavailable. Other product information remains available.