Dosage and administration
Place enough product on hands to cover all surfaces. Rub together until dry. Supervise children under 6 years when using this product to avoid swallowing
ESTEE LAUDER HAND SANITIZER
- Manufacturer
- ESTEE LAUDER INC | Whitman Laboratories Ltd. | ESTEE LAUDER COMPANY, THE | Estee Lauder Cosmetics Ltd. | Estee Lauder N.V. | NORTHTEC INC | NORTHTEC PALC | Len-Ron Manufacturing Division of Aramis Inc. | PADC 1
- Effective date
- 2021-07-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:18:09
Label at a glance#
ProductESTEE LAUDER HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections
Storage and handling
Store between 59-86F Avoid freezing and excessive heat above 104F
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only
Flammable. Keep away from fire or flame.
Do not use
- on children under 2 months
- on open skin wounds
OTC - WHEN USING SECTION
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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
- Place enough product on hands to cover all surfaces. Rub together until dry.
- Supervise children under 6 years when using this product to avoid swallowing
Other information
- Store between 59-86F
- Avoid freezing and excessive heat above 104F
Inactive ingredients
water\aqua\eau • acrylates/c10-30 alkyl acrylate crosspolymer • aminomethyl propanol • methyl gluceth-20 • t-butyl alcohol <iln48831>
PRINCIPAL DISPLAY PANEL - 8.5 FL. OZ. Bottle Label
ESTĒE LAUDER
Hand Sanitizer
Ethyl Alcohol 70%
Antiseptic Hand Sanitizer
Non-sterile Solution
8.5 FL. OZ.
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 11559-059-01 | 2021-07-27 | C162847 | 48780-1 | c7ccaba7-1a0d-fd44-e053-dadaa90aa01b | ESTĒE LAUDER HAND SANITIZER |
| 11559-059-01 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-1a0d-fd44-e053-dadaa90aa01b | ESTĒE LAUDER HAND SANITIZER |
Products#
Every source-derived product name is available through these pages.
- ESTEE LAUDER HAND SANITIZER
- ALCOHOL
- WATER
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- AMINOMETHYLPROPANOL
- METHYL GLUCETH-20
- TERT-BUTYL ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11559-059 | 11559-059-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) | 59TL3WG5CO | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| METHYL GLUCETH-20 | J3QD0LD11P | IACT |
| TERT-BUTYL ALCOHOL | MD83SFE959 | 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 |
|---|---|---|---|---|---|---|
| 52120ee1-dee2-4ede-b4b4-c36e9093acfd | a3e67e9e-0da5-46e6-8c18-a34b1a74ee05 | 2021-07-27 | Warnings | 52120ee1-dee2-4ede-b4b4-c36e9093acfd a3e67e9e-0da5-46e6-8c18-a34b1a74ee05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.