FLORA SHINE ALCOHOL ANTI-BACTERIAL- alcohol cloth

Flora Shine Alcohol Anti-Bacterial by

Drug Labeling and Warnings

Flora Shine Alcohol Anti-Bacterial by is a Otc medication manufactured, distributed, or labeled by EasyPort USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient Alcohol 75%

PURPOSE

Purpose Antimicrobial

INDICATIONS & USAGE

Uses Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only

Flammable. Keep away from fire or flame

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

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• 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

Inactive ingredients Water, glycerin

Other information

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

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FLORA SHINE ALCOHOL ANTI-BACTERIAL 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81454-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81454-100-10	100 in 1 CANISTER	01/11/2021
1		350 mL in 1 CANISTER; Type 0: Not a Combination Product
2	NDC: 81454-100-06	60 in 1 PACKAGE	01/11/2021
2		285 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/11/2021

Labeler - EasyPort USA LLC (023373118)