Indications and uses
Sanitizer to help reduce bacteria on skin. For use when water is not available.
Refresher
- Manufacturer
- Jao Limited | Fragrance Manufacturing, Inc.
- Effective date
- 2025-06-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 15
- Source
- full-release
- Hydrated at
- 2026-06-01 01:38:17
Label at a glance#
ProductRefresher
Active ingredientALCOHOL
Label structure11 sections
Dosage and administration
Apply on hands, rub briskly until dry.
Contacts and useful links#
Websitewww.jaobrand.com
WWW.JAOBRAND.COM
WWW.JAOBRAND.COMLabel contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 65%
Purpose
Antimicrobial
Uses:
Sanitizer to help reduce bacteria on skin.
For use when water is not available.
Warnings
For external use only. Flammable.
Keep away from heat or flame.
When using this product
- Keep out of eyes. In case of contact, flush thoroughly with water.
- Avoid contact with broken skin.
Stop and ask a doctor
if irritation develops.
Keep out of reach of children.
If swallowed get medical help or contact Poison Control Center right away.
Directions
Apply on hands, rub briskly until dry.
Other Info
- Do not store above 100 oF (43 oC).
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis, Amino-Methyl Propanol, Calendula Extract, Chamomile Extract, dl-Panthenol, Essential Oils (Lavender, Tea Tree, Eucalyptus, Geranium, Clary Sage), Glycerine and Glyceryl Polyacrylate, PPG-20 Methyl Glucose Ether Distearate, Water
PRINCIPAL DISPLAY PANEL
JAO®
REFRESHER
NOT JUST FOR HANDS
MULTIPURPOSE
SANITIZER
8 fl oz/236 ml ℮ ∙ Made in USA
Distributed by JAO Ltd Lansdale, PA 19446
©JAO Ltd 888 296 8685 MADE IN USE
WWW.JAOBRAND.COM
Label
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69662-111-01 | Refresher | 236 mL in 1 BOTTLE, PUMP | LIQUID | 236 | 15 | |
| 69662-111-02 | Refresher | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 15 | |
| 69662-111-03 | Refresher | 118 mL in 1 BOTTLE, SPRAY | LIQUID | 118 | 15 | |
| 69662-111-04 | Refresher | 3750 mL in 1 JUG | LIQUID | 3750 | 15 | |
| 69662-111-05 | Refresher | 840 mL in 1 POUCH | LIQUID | 840 | 15 |
Products#
Every source-derived product name is available through these pages.
- Refresher
- alcohol
- ALOE VERA LEAF
- GLYCERIN
- PANTHENOL
- ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (LOW ALLYL METHACRYLATE)
- AMINOMETHYLPROPANOL
- CHAMOMILE
- CALENDULA ARVENSIS LEAF
- ACETYLATED SUCROSE DISTEARATE
- LAVENDER OIL
- EUCALYPTUS OIL
- WATER
- GERANIUM OIL, ALGERIAN TYPE
- SAGE OIL
- GREEN TEA LEAF
- POLYSORBATE 20
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69662-111 | 69662-111-01, 69662-111-02, 69662-111-03, 69662-111-04, 69662-111-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 14 | 2024-01-04 | full-release | 2026-06-01 00:06:38 |
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 |
|---|---|---|---|---|---|---|
| Refresher | ALCOHOL | Jao Limited | 1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8 | 2025-06-13 | Warnings | 69662-111-04 69662-111-01 69662-111-05 69662-111-02 69662-111-03 69662-111 69662011101 69662011104 69662011102 69662011103 69662011105 37771115-d2fc-88e3-e063-6394a90aab56 1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.