Indications and uses
Hand sanitizer to help reduce bacteria on the skin
PURELL Advanced Hand Sanitizer Soothing Gel
- Manufacturer
- GOJO Industries, LLC | The Travis Association for the Blind
- Effective date
- 2026-07-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- daily-update
- Hydrated at
- 2026-07-17 21:45:42
Label at a glance#
ProductPurell Advanced Soothing
Active ingredientALCOHOL
Label structure7 sections
Dosage and administration
Put enough product in your palm to cover hands and rub hands together briskly until dry Children under 6 years of age should be supervised when using PURELL
Contacts and useful links#
Websitewww.purell.com
www.PURELL.com
www.PURELL.comLabel contents#
Full prescribing information#
Active ingredient
Ethyl alcohol 70% v/v
Purpose
Antimicrobial
Uses
- Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
For external use only
OTC - WHEN USING SECTION
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash appears and lasts
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
- Put enough product in your palm to cover hands and rub hands together briskly until dry
- Children under 6 years of age should be supervised when using PURELL
Inactive ingredients
Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)
Distributed by: GOJO Industries, Inc. Akron, OH 44309
Questions? Tel: 1-888-4-PURELL ￭ www.PURELL.com
©2011, GOJO Industries, Inc.
All rights reserved. Made in U.S.A.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Purell Advanced Soothing
- alcohol
- WATER
- ISOPROPYL ALCOHOL
- ALOE VERA LEAF
- CAPRYLYL GLYCOL
- GLYCERIN
- ISOPROPYL MYRISTATE
- .ALPHA.-TOCOPHEROL ACETATE, D-
- AMINOMETHYLPROPANOL
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 5
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 21749-713 | 21749-713-01, 21749-713-02, 21749-713-04, 21749-713-08, 21749-713-10, 21749-713-12, 21749-713-20, 21749-713-27, 21749-713-28, 21749-713-33, 21749-713-40, 21749-713-67, 21749-713-65, 21749-713-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| CAPRYLYL GLYCOL | 00YIU5438U | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, D- | A7E6112E4N | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 7 | 2024-12-11 | full-release | 2026-06-01 00:42:26 |
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 |
|---|---|---|---|---|---|---|
| Purell Advanced Soothing | ALCOHOL | GOJO Industries, LLC | 59b47629-8b4e-4084-8bc8-66c7e5599e9c | 2026-07-10 | Warnings | 21749-713-10 21749-713-28 21749-713-08 21749-713-65 21749-713-67 21749-713-20 21749-713-04 21749-713-33 21749-713-02 21749-713-24 21749-713-27 21749-713-40 21749-713-01 21749-713-12 21749-713 21749071365 21749071324 21749071308 21749071333 21749071340 21749071304 21749071328 21749071327 21749071312 21749071310 21749071301 21749071320 21749071302 21749071367 5643056c-a2b5-b48a-e063-6394a90a6a5d 59b47629-8b4e-4084-8bc8-66c7e5599e9c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.