Flora Shine Alcohol Free Anti-Bacterial

Manufacturer
EasyPort USA LLC
Effective date
2021-01-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:55:17

Label at a glance#

ProductFlora Shine Alcohol Free Anti-Bacterial
Active ingredientBENZALKONIUM CHLORIDE
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 Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose Antimicrobial

INDICATIONS & USAGE SECTION

Uses Hand sanitizer to help reduce bacteria on the skin

WARNINGS SECTION

Warnings For external use only

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, cetylpyridinium chloride, chlorphenesin, ethylhexylglycerin, propylene glycol, glycerol

Other information

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

FLORA SHINE

FRAGRANCE FREE

ALCOHOL FREE

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 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81454-30081454-300-08, 81454-300-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
2c683253-3c97-0c10-e063-6294a90adb8fb8baf72c-0d22-835c-e053-2a95a90a03602025-01-01WarningsExact identifier
spl set id: b8baf72c-0d22-835c-e053-2a95a90a0360

Reported adverse events (FAERS/openFDA)#

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