FDA.reportPublic FDA data

Refrasia Care Hand Sanitizer

Manufacturer
Lemon X dba The Bevolution Group
Effective date
2020-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:22

Label at a glance#

ProductRefrasia Care Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information Store below 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • Hand sanitizer to help reduce bacteria that can potentially cause disease
  • Recommended for repeated use

WARNINGS SECTION

Warnings
For external use only
Flammable. Keep away from heat or flame

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last 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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally to hands to cover all surfaces
  • Rub hands together until dry
  • Supervise children under 6 years old
  • Not recommended for infants

STORAGE AND HANDLING SECTION

Other information

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive ingredients

Propylene Glycol, Purified Water, Xanthan Gum

OTC - QUESTIONS SECTION

Questions? (800) 628-6449

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

refrasia ™ care

Hand Sanitizer

Kills 99.9% of Germs

bevolution group®

MANUFACTURED BY BEVOLUTION GROUP™

FROSTPROOF, FL 33843

1-800-628-6449

bevolutiongroup.com

64 FL. OZ. (1/2 GAL) 1.9L

Bevolution HS FrontBevolution HS Front

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75080-00175080-001-02, 75080-001-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
XANTHAN GUMTTV12P4NEEIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
cfe9207a-144e-6101-e053-2a95a90a698ca2f65fcd-e9fb-7707-e053-2a95a90acebe2021-11-03WarningsExact identifier
spl set id: a2f65fcd-e9fb-7707-e053-2a95a90acebe

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.