Flora Shine Alcohol Anti-Bacterial

Manufacturer
EasyPort USA LLC
Effective date
2021-01-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:55:18

Label at a glance#

ProductFlora Shine Alcohol Anti-Bacterial
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Rub wipe thoroughly over all surfaces of both hands and allow to dry Supervise children under 6 years old Not recommended for infants Dispose of wipe in trash; do not flush

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Alcohol 75%

OTC - PURPOSE SECTION

Purpose Antimicrobial

INDICATIONS & USAGE SECTION

Uses Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub wipe thoroughly over all surfaces of both hands and allow to dry
  • Supervise children under 6 years old
  • Not recommended for infants
  • Dispose of wipe in trash; do not flush

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, glycerin

Other information

SPL UNCLASSIFIED SECTION

Store in cool and dry place, keep awway from heat and direct sunlight

SPL UNCLASSIFIED SECTION

FLORA SHINE

FRAGRANCE FREE

75% ALCOHOL

ANTI-BACTERIAL Wipes

Mfg. Exclusively For:

Offshore International Paper

Austin, TX 78704

Toll Free:

(833) 697-2737

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81454-10081454-100-10, 81454-100-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB

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
2c682545-b4f9-0447-e063-6394a90ab6cfb8ccf578-f613-7ef8-e053-2995a90a57662025-01-01WarningsExact identifier
spl set id: b8ccf578-f613-7ef8-e053-2995a90a5766

Reported adverse events (FAERS/openFDA)#

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