Indications and uses
For handwashing to decrease bacteria on the skin.
Peeps - Vanilla Marshmallow Puff Hand Sanitizer (76891-192-07)
- Manufacturer
- Scent Theory Products LLC
- Effective date
- 2026-09-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-09-22 03:02:57
Label at a glance#
ProductPeeps - Vanilla Marshmallow Puff Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections
Dosage and administration
Spray hands with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants
Label contents#
Full prescribing information#
Active ingredients
Ethyl Alcohol 62% V/V
Purpose
Antibacterial
Uses
For handwashing to decrease bacteria on the skin.
Warnings
For external use only: hands
Flammable, keep away from fire or flame.
OTC - WHEN USING SECTION
When using this product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- avoid contact with broken skin.
- do not inhale or ingest.
OTC - STOP USE SECTION
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
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
Spray hands with product and allow to dry without wiping
For children under 6, use only under adult supervision
Not recommended for infants
Other information
Do not store above 105°F
may discolor some fabrics
harmful to wood finishes and plastics
Inactive ingredients
Water (Aqua), Aloe Barbadensis Extract, Glycerin, Fragrance (Parfum), Eucalyptus Globulus Leaf Oil, Denatonium Benzoate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Label
Products#
Every source-derived product name is available through these pages.
- Peeps - Vanilla Marshmallow Puff Hand Sanitizer
- Alcohol
- WATER
- ALOE VERA LEAF
- GLYCERIN
- EUCALYPTUS GLOBULUS LEAF
- DENATONIUM BENZOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76891-192 | 76891-192-07 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| EUCALYPTUS GLOBULUS LEAF | S546YLW6E6 | IACT |
| DENATONIUM BENZOATE | 4YK5Z54AT2 | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.